| 1 | Mexican geneticists' views of ethical issues in genetics testing and screening. Are eugenic principles involved? | Coautor y autor de correspondencia: Armendares S., Lisker R., Carnevale A. | 1999 | CLINICAL GENETICS | WoS-id: 000084168800013
Scopus-id: 2-s2.0-0032724159
| 6 | 7 |
| 2 | Attitudes of Mexican geneticists towards prenatal diagnosis and selective abortion | Coautor: Armendares S., Carnevale A., Lisker R., Villa A.R. | 1998 | AM J MED GENET | WoS-id: 000071776800016
Scopus-id: 2-s2.0-0032477708
| 16 | 16 |
| 3 | Mexican geneticists' opinions on disclosure issues | Coautor: Armendares S., Lisker R., Carnevale A., Villa J.A., et al. | 1998 | CLINICAL GENETICS | WoS-id: 000076697400009
Scopus-id: 2-s2.0-0031725174
| 8 | 11 |
| 4 | Genetic disorders of the adult age [Padecimientos genéticos de la edad adulta.] | 2ᵒ autor: Armendares S., Salamanca-Gómez F., Alonso-Vilatela M.E., Kofman-Alfaro S., et al. | 1996 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0030185771
| 0 | 0 |
| 5 | Genetic influence on energy requirements. III. Multifactorial inheritance modified by gender [Influencia genética en requerimientos de energía. III. Herencia multifactorial modulada por género.] | 1ᵉʳ autor: Armendares S., Cravioto J., Frías M., Galván F. | 1995 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1995TF40500003
Scopus-id: 2-s2.0-0029367069
| 0 | 0 |
| 6 | Utilization of dietary energy in the rat. IV. Multifactorial inheritance modulated by gender | 1ᵉʳ autor: Armendares S., Cravioto J., Frias M., Galvan F. | 1995 | Archives Of Medical Research | WoS-id: A1995UM15800026
Scopus-id: 2-s2.0-0029587436
| 1 | 1 |
| 7 | The development of human genetics in Mexico | 2ᵒ autor y autor de correspondencia: Armendares S., Salamanca F. | 1995 | Archives Of Medical Research | WoS-id: A1995UM15800012
Scopus-id: 2-s2.0-0029616320
| 2 | 1 |
| 8 | Polymorphisms of chromosomes 1, 9, and 16 in Mexican mestizos [Polimorfismos de los cromosomas 1, 9 y 16 en mestizos mexicanos.] | 1ᵉʳ autor: Armendares S., Buentello L., Gaona O., Salamanca F., et al. | 1993 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1993LE23000005
Scopus-id: 2-s2.0-0027571801
| 1 | 0 |
| 9 | The present frontiers of human genetics [Fronteras actuales de la genética humana.] | 2ᵒ autor: Armendares S., Salamanca Gómez F., Lisker R. | 1992 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0026951317
| 0 | 0 |
| 10 | Genetic influence on energy requirements. I. Development of an experimental model [Influencia genética sobre los requerimientos de energia. I. Desarrollo de un modelo experimental.] | Coautor: Armendares S., Cravioto J., Vizcaíno G., Frías M., et al. | 1992 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1992JU54000001
Scopus-id: 2-s2.0-0026894630
| 1 | 0 |
| 11 | Genetic disorders in sexual differentiation in humans [Trastornos genéticos de la diferenciación sexual en el humano.] | Coautor: Armendares S., Salamanca-Gómez F., Kofman-Alfaro S.H., Cuevas-Covarrubias S.A., et al. | 1992 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0026449139
| 0 | 1 |
| 12 | The heredity of obesity. Epidemiologic evidence (1923-1990) [La herencia de la obesidad. Evidencia epidemiológica. (1923-1990).] | 1ᵉʳ autor y autor de correspondencia: Armendares S. | 1991 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1991GZ62300013
Scopus-id: 2-s2.0-0026184961
| 0 | 0 |
| 13 | Human genetics in Mexico [La génetica humana en México.] | 2ᵒ autor: Armendares S., Kofman-Alfaro S., Carnevale A., Salamanca-Gómez F., et al. | 1991 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0025717798
| 0 | 1 |
| 14 | Frequency of mixoploidy in 85 index cases with Down syndrome [Frecuencia de mixoploidías en 85 casos índice con síndrome de Down.] | 1ᵉʳ autor: Armendares S., Buentellos L., Salamanca F. | 1990 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1990DT25700005
Scopus-id: 2-s2.0-3242850184
| 1 | 2 |
| 15 | Cytogenetic study of the parents of 85 index cases with regular trisomy 21 [Estudio citogenético en los progenitores de 85 casos índice con trisomía 21 regular.] | 1ᵉʳ autor: Armendares S., Buentello L., Salamanca F. | 1990 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1990DY32200003
Scopus-id: 2-s2.0-0025451619
| 1 | 3 |
| 16 | Usefulness of chromosomal heteromorphisms obtained by G-banding for identification of illegitimacy [Utilidad de los heteromorfismos cromosómicos obtenidos por bandas G para la identificación de ilegitimidad.] | 1ᵉʳ autor: Armendares S., Buentello L., Salamanca F., Lisker R. | 1990 | Archivos De Investigación Médica | WoS-id: A1990FY83400017
Scopus-id: 2-s2.0-0025415465
| 0 | 0 |
| 17 | Down's syndrome and illegitimacy [Sindrome de Down e ilegitimidad.] | 1ᵉʳ autor: Armendares S., Buentello L., Lisker R., Pérez-Briceño R. | 1987 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1987J499200010
Scopus-id: 2-s2.0-0023321212
| 2 | 0 |
| 18 | Heterochromatin C sizes distribution of chromosomes 1, 9, 16 and Y in a sample of the Mexican population: comparison of two quantitative methods of measurement. | Coautor: Armendares S., Mutchinick O., Sánchez F., Lisker R., et al. | 1987 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1987J499200004
Scopus-id: 2-s2.0-0023321995
| 1 | 0 |
| 19 | Gene frequencies and admixture estimates in a Mexico City population | Coautor: Armendares S., Lisker R., Perez-Briceño R., Granados J., et al. | 1986 | AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY | WoS-id: A1986E621200006
Scopus-id: 2-s2.0-0022490058
| 99 | 107 |
| 20 | A patient with 44 chromosomes | Coautor: Armendares S., Salamanca F., Buentello L., Sanchez J. | 1985 | ANN GENET-PARIS | WoS-id: A1985AMV9000016
Scopus-id: 2-s2.0-0021845735
| 9 | 7 |
| 21 | Sensitivity of 6 genetic markers for the identification of illegitimacy in Mexico City [Sensibilidad de seis marcadores genéticos para la identificación de ilegitimidad en la Ciudad de México.] | 1ᵉʳ autor: Armendares S., Lisker R., Pérez Briceño R., Buentello L. | 1985 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1985AGR8100006
Scopus-id: 2-s2.0-0021942838
| 3 | 2 |
| 22 | Absence of correlation between Y chromosome heterochromatin and several anthropometric measurements in a Mexican population | 1ᵉʳ autor: Armendares S., Lisker R., Mutchinick O., Sánchez F., et al. | 1983 | HUMAN GENETICS | Scopus-id: 2-s2.0-0020511985
| 0 | 2 |
| 23 | Defective monocyte chemotaxis in children with down?s syndrome | Coautor: Armendares S., Barroeta O., Nungaray L., Lopez-Osuna M., et al. | 1983 | PEDIATRIC RESEARCH | WoS-id: A1983QJ21600013
Scopus-id: 2-s2.0-0020673633
| 28 | 27 |
| 24 | Experience in a private cytogenetics laboratory (author's transl) [Experiencia de un laboratorio privado de citogenética médica.] | 1ᵉʳ autor: Armendares S., Buentello L., Nava S., Salamanca F. | 1982 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1982NJ39200005
Scopus-id: 2-s2.0-0020009940
| 0 | 0 |
| 25 | Human identity [La identidad del hombre.] | Coautor: Armendares S., Campillo-Sainz C., Xirau R., Kretschmer R., et al. | 1982 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0020186836
| 0 | 0 |
| 26 | Altered carbohydrate content of IgG in asymptomatic smokers. | Coautor: Armendares S., Rostenberg I., Peñaloza R., Guízar Vázquez J., et al. | 1981 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1981LH82800008
Scopus-id: 2-s2.0-0019343682
| 0 | 0 |
| 27 | Brief clinical report: An XXXYY male | Coautor: Armendares S., Salamanca-Gomez F., Cortes R., Sanchez J. | 1981 | AM J MED GENET | WoS-id: A1981MV78300005
Scopus-id: 2-s2.0-0019785454
| 9 | 4 |
| 28 | Chromosome studies of bone marrow cells from metronidazole-treated patients | Coautor: Armendares S., Salamanca-Gomez F., Castaneda G., Farfan J., et al. | 1980 | ANN GENET-PARIS | WoS-id: A1980JN28000015
Scopus-id: 2-s2.0-0018842115
| 11 | 7 |
| 29 | Frequency of sister chromatid exchanges in severe protein calorie malnutrition | Coautor: Armendares S., Mutchinick O., Lisker R., Ruz L., et al. | 1979 | ANN GENET-PARIS | WoS-id: A1979HW05200002
Scopus-id: 2-s2.0-0018712958
| 19 | 17 |
| 30 | Association on Sturge Weber and Klippel Trenaunay Weber syndromes. Apropos of 2 cases [Asociación de los síndromes de Sturge-Weber y Klippel-Trenaunay-Weber. A propósito de dos casos.] | Coautor: Armendares S., Guízar Vázquez J., Navarrete Cadena C., Barrón Uribe C., et al. | 1979 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-0018470917
| 0 | 0 |
| 31 | Haptoglobin phenotypes and antibodies against measles. | Coautor: Armendares S., Rostenberg I., Ruíz-Gómez J., Núñez C., et al. | 1979 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1979HS37400012
Scopus-id: 2-s2.0-0018490841
| 0 | 0 |
| 32 | Atherosclerosis. Genetic aspects [Aterosclerosis. III Aspectos geneticos.] | 1ᵉʳ autor y autor de correspondencia: Armendares S. | 1979 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0018626887
| 0 | 0 |
| 33 | Partial 2p trisomy (p21?pter) in two siblings of a family with a 2p-:15q+ translocation | 1ᵉʳ autor: Armendares S., Salamanca-Gómez F. | 1978 | CLINICAL GENETICS | WoS-id: A1978EL01300003
Scopus-id: 2-s2.0-0017855558
| 29 | 19 |
| 34 | Survey on the training in human sexuality matters required in medical schools of the Mexican Republic [Encuesta sobre el adiestramiento que en materia de sexualidad humana se imparte en las escuelas y facultades de medicina de la República | 2ᵒ autor y autor de correspondencia: Armendares S., Brostein de Ranen E. | 1978 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0017986496
| 0 | 0 |
| 35 | Growth effect of oxandrolone in patients with Turner's syndrome (author's transl) [Effecto de la oxandrolona sobre el crecimiento en pacientes con sindrome de Turner.] | 1ᵉʳ autor: Armendares S., Ramos R.M., Navarrete C., Salamanca F. | 1978 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1978GJ50800005
Scopus-id: 2-s2.0-0018023153
| 1 | 0 |
| 36 | Congenital spondyloepiphyseal dysplasia. Apropos of a case [Displasia espondiloepifisial congénita. A propósito de un case.] | Coautor: Armendares S., Guízar Vázquez J., Arredondo Vega F., Manzano C. | 1978 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-0018040447
| 0 | 0 |
| 37 | Microtia and meatal atresia in mother and son | Coautor: Armendares S., Guizar Vazquez J., Arredondo Vega F., Rostenberg I., et al. | 1978 | CLINICAL GENETICS | WoS-id: A1978FQ25400004
Scopus-id: 2-s2.0-0018180406
| 21 | 17 |
| 38 | Characterization of the new syndromes of genetic origin [Contribución a la caracterización de nuevos sindromes de índole genética.] | 1ᵉʳ autor: Armendares S., Salamanca F. | 1977 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0017513511
| 0 | 0 |
| 39 | Pycnodysostosis. Five cases in three mexican families (author's transl) [Picnodisostósis. Descripción de cinco casos en tres familias mexicanas.] | Coautor: Armendares S., Guízar-Vázquez J., Navarrete-Cadena C., Manzano C., et al. | 1977 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1977EE57000008
Scopus-id: 2-s2.0-0017542868
| 4 | 3 |
| 40 | Clinical and cytogenetic findings in 74 patients with Turner's syndrome seen in a pediatric hospital (author's transl) [Hallazgos clínicos y cromosómicos en 74 pacientes con sindrome de Turner atendidas en un hospital de pediatria.] | 1ᵉʳ autor: Armendares S., Salamanca F. | 1977 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1977EE57000005
Scopus-id: 2-s2.0-0017549084
| 5 | 2 |
| 41 | Human genetics | 1ᵉʳ autor: Armendares S., Lisker R. | 1977 | American Society Of Mechanical Engineers (paper) | Scopus-id: 2-s2.0-0017621721
| 0 | 0 |
| 42 | Intrafamilial correlation analysis for IgM serum levels | Coautor: Armendares S., Guizar-Vazquez J., Saint-Martin F.P., Rostenberg I., et al. | 1977 | AMERICAN JOURNAL OF HUMAN GENETICS | WoS-id: A1977EC27000003
Scopus-id: 2-s2.0-0017705229
| 10 | 7 |
| 43 | Dwarfism, mental retardation, facial dysplasia, macrophthalmia and lens opacities: Case report 58 | Coautor y autor de correspondencia: Armendares S., Cantu J.M., Hernandez A. | 1977 | Syndrome Identification | Scopus-id: 2-s2.0-0017715035
| 0 | 0 |
| 44 | Chromosome studies in azoospermic patients (author's transl) [Estudios cromosómicos en pacientes azoospérmicos] | 1ᵉʳ autor: Armendares S., Giner J., Merino G., Salamanca F. | 1976 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1976CS30500003
Scopus-id: 2-s2.0-0017008297
| 2 | 0 |
| 45 | A contribution of new cytogenetic techniques to the knowledge of chromosomal abnormalities (author's transl) [Contribución de las nuevas técnicas citogenéticas al conocimiento de las anormalidades cromosómicas] | 2ᵒ autor y autor de correspondencia: Armendares S., Salamanca-Gómez F. | 1976 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1976CS30500010
Scopus-id: 2-s2.0-0017008247
| 0 | 0 |
| 46 | Familial true hermaphrodism in three siblings: plasma hormonal profile and in vitro steroid biosynthesis in gonadal structures | Coautor y autor de correspondencia: Armendares S., Gallegos A.J., Guizar E. | 1976 | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | WoS-id: A1976BN60300006
Scopus-id: 2-s2.0-0017110838
| 11 | 11 |
| 47 | Potential fertility in incomplete male pseudohermaphroditism type 2. | Coautor: Armendares S., Cantú J.M., Hernández-Montes H., Del Castillo V., et al. | 1976 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1976BX21800010
Scopus-id: 2-s2.0-0016945255
| 20 | 18 |
| 48 | Ten years experience in a cytogenetics laboratory of a large medical center (author's transl) [Experiencia de diez años de trabajo de un laboratorio de citogenetica medica] | 1ᵉʳ autor: Armendares S., Salamanca F., Buentello L., Sanchez J., et al. | 1976 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1976BX21800003
Scopus-id: 2-s2.0-0016949030
| 3 | 1 |
| 49 | Somatometric profile in patients with Turner syndrome. | Coautor y autor de correspondencia: Armendares S., Ramos R.M., Rostenberg I. | 1976 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1976CU13600003
Scopus-id: 2-s2.0-0016974768
| 1 | 0 |
| 50 | The effect of the family environment on the psychological characteristics of patients with Turner's syndrome. I. The Wechsler and Bender tests [Influencia del medio ambiente familiar sobre ciertas características psicológicas de las pacien | 2ᵒ autor y autor de correspondencia: Armendares S., Brostein E. | 1976 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1976CU13600002
Scopus-id: 2-s2.0-0016974770
| 2 | 0 |
| 51 | Role of the anithyroideal antibodies in the etiology of chromosome aberrations [Papel de los Anticuerpos antitiroideos en la etiologia de las aberraciones chromosómicas] | Coautor: Armendares S., Lisker R., Fialkow P.J., Zavala C. | 1976 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0016987083
| 0 | 1 |
| 52 | Preventive aspects in human genetics [ASPECTOS PREVENTIVOS EN GENETICA HUMANA] | 1ᵉʳ autor y autor de correspondencia: Armendares S. | 1976 | Anuario De Actualizacion En Medicina | Scopus-id: 2-s2.0-0017209285
| 0 | 0 |
| 53 | Identification of partial 2p trisomy [FIFTH INTERNATIONAL CONGRESS OF HUMAN GENETICS] | Coautor: Armendares S., Salamanca Gomez F., Sanchez J., Fragoso R. | 1976 | Excerpta Med., Amsterdam, I.C.S. | Scopus-id: 2-s2.0-18544397055
| 0 | 0 |
| 54 | Human acrocentric ring chromosomes and satellite association | Coautor: Armendares S., Cantu J.M., Salamanca F., Sanchez J., et al. | 1975 | ANN GENET-PARIS | WoS-id: A1975AS59600008
Scopus-id: 2-s2.0-0016765768
| 13 | 6 |
| 55 | Banding in old chromosome preparations | 2ᵒ autor y autor de correspondencia: Armendares S., Salamanca F. | 1975 | ANN GENET-PARIS | WoS-id: A1975AJ23600012
Scopus-id: 2-s2.0-0016745458
| 1 | 0 |
| 56 | The 12p trisomy syndrome | 1ᵉʳ autor: Armendares S., Salamanca F., Nava S., Ramirez S., et al. | 1975 | ANN GENET-PARIS | WoS-id: A1975AJ23600002
Scopus-id: 2-s2.0-0016715326
| 38 | 24 |
| 57 | Identification of isochromosome 17 in a girl with mental retardation and congenital malformation | 2ᵒ autor y autor de correspondencia: Armendares S., Salamanca Gomez F. | 1975 | ANN GENET-PARIS | WoS-id: A1975BE12600005
Scopus-id: 2-s2.0-0016789212
| 17 | 9 |
| 58 | Twinning and cleft lip with or without cleft palate | 1ᵉʳ autor: Armendares S., Lisker R. | 1975 | JOURNAL OF PEDIATRICS | WoS-id: A1975V727000036
Scopus-id: 2-s2.0-0016475853
| 3 | 3 |
| 59 | The Norrie's disease (author's transl) [La enfermedad de Norre] | Coautor: Armendares S., Hernández A., Cantú J.M., Rojas J. | 1975 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1975AF45300008
Scopus-id: 2-s2.0-0016492432
| 1 | 1 |
| 60 | Genetic analysis in families with histidinemía (author's transl) [Análisis genético en familias con histidinemia] | Coautor y autor de correspondencia: Armendares S., Rostenberg I., Guízar-Vázquez J. | 1975 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1975AS28000008
Scopus-id: 2-s2.0-0016526108
| 0 | 0 |
| 61 | Ring chromosome 6 in a malformed boy | Coautor y autor de correspondencia: Armendares S., Salamanca-Gonez F., Nava S. | 1975 | CLINICAL GENETICS | WoS-id: A1975BA26000010
Scopus-id: 2-s2.0-0016644014
| 38 | 32 |
| 62 | Lower lip and cleft lip with "pits" (Van der Woude syndrome). Study in a family (author's transl) [Labio y paladar hendidos con "fosetas" labiales (sindrome de Van der Woude). Estudio de una familia] | 2ᵒ autor y autor de correspondencia: Armendares S., Guízar-Vázquez J. | 1975 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1975BG76800008
Scopus-id: 2-s2.0-0016564768
| 1 | 0 |
| 63 | A newly recognized inherited syndrome of dwarfism, craniosynostosis, retinitis pigmentosa and multiple congenital malformations [NEW CHROMOSOMAL AND MALFORMATION SYNDROMES] | 1ᵉʳ autor: Armendares S., Antillon F., Del Castillo V., Jimenez M. | 1975 | Birth Defects, Orig.Art.Ser. | Scopus-id: 2-s2.0-0016830548
| 0 | 0 |
| 64 | Familial true hermaphrodism in three siblings - Clinical, cytogenetic, histological and hormonal studies | 1ᵉʳ autor: Armendares S., Salamanca F., Cantú J.M., del Castillo V., et al. | 1975 | HUMAN GENETICS | WoS-id: A1975AQ36500002
Scopus-id: 2-s2.0-0016716443
| 26 | 21 |
| 65 | Oculodentodigital dysplasia (author's transl) [Displasia oculodentodigital] | Coautor y autor de correspondencia: Armendares S., Guízar-Vázquez J., Rostenberg I. | 1975 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1975AG14100009
Scopus-id: 2-s2.0-0016422484
| 4 | 5 |
| 66 | A case of trisomy 18 with bilateral absence of thumbs and aplasia of the left radius [Un caso de trisomía 18 con ausencia de ambos pulgares y aplasia del radio izquierdo] | 1ᵉʳ autor: Armendares S., Salamanca F., Cortés R. | 1975 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-0016454330
| 0 | 0 |
| 67 | Somatometry of the face in preschool children [NEW CHROMOSOMAL AND MALFORMATION SYNDROMES] | Coautor: Armendares S., Rostenberg I., Jimenez M., Daltabuit M. | 1975 | Birth Defects: Original Article Series | Scopus-id: 2-s2.0-0016758964
| 0 | 0 |
| 68 | Absence of pectoralis major muscle in 2 sisters associated with leukemia in one of them [NEW CHROMOSOMAL AND MALFORMATION SYNDROMES] | 1ᵉʳ autor: Armendares S., Rostenberg I. | 1975 | Birth Defects, Orig.Art.Ser. | Scopus-id: 2-s2.0-0016777412
| 0 | 1 |
| 69 | Reply | 1ᵉʳ autor: Armendares S., Lisker R., Genética S.d. | 1975 | JOURNAL OF PEDIATRICS | WoS-id: A1975AV38900051
Scopus-id: 2-s2.0-58149405897
| 0 | 0 |
| 70 | Genetic component and children mortality (author's transl) [El componente genético en la mortalidad infantil] | 1ᵉʳ autor: Armendares S., Cortés R., de la Rosa L. | 1974 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1974T383900002
Scopus-id: 2-s2.0-0015946330
| 8 | 6 |
| 71 | Contribution of hereditary factors in human pathology [Contribución de los factores hereditarios en la patología humana] | 1ᵉʳ autor y autor de correspondencia: Armendares S. | 1974 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0016052266
| 0 | 0 |
| 72 | Current status of the knowledge of the effect of malnutrition on the genetic material [Estado actual de los conocimientos del effecto de la desnutrición sobre el material genético] | 1ᵉʳ autor: Armendares S., Salamanca F., Frenk S. | 1974 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0016053281
| 0 | 1 |
| 73 | The development of genetics [El desarrollo de la genética] | 1ᵉʳ autor y autor de correspondencia: Armendares S. | 1974 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | Scopus-id: 2-s2.0-0016053427
| 0 | 0 |
| 74 | Facioacromelic disostosis with metal retardation (author's transl) [Acrodisostósis. Disostoósis facio-acromélica con retardo mental] | Coautor: Armendares S., Cantú J.M., Hernández A., Nazará-Cazorla Z., et al. | 1974 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1974U464900007
Scopus-id: 2-s2.0-0016085023
| 0 | 0 |
| 75 | Absence of pectoralis major muscle in two sisters associated with leukemia in one of them | 1ᵉʳ autor y autor de correspondencia: Armendares S. | 1974 | JOURNAL OF PEDIATRICS | WoS-id: A1974U009300034
Scopus-id: 2-s2.0-0016107829
| 25 | 16 |
| 76 | A newly recognized inherited syndrome of dwarfism, craniosynostosis, retinitis pigmentosa, and multiple congenital malformations | 1ᵉʳ autor: Armendares S., Antillon F., Del Castillo V., Jimenez M. | 1974 | JOURNAL OF PEDIATRICS | WoS-id: A1974U815100034
Scopus-id: 2-s2.0-0016140827
| 3 | 3 |
| 77 | C bands in human metaphase chromosomes treated by barium hydroxide | 2ᵒ autor y autor de correspondencia: Armendares S., Salamanca F. | 1974 | ANN GENET-PARIS | WoS-id: A1974T569000014
Scopus-id: 2-s2.0-0016156825
| 177 | 126 |
| 78 | Leukocyte function in Down's syndrome quantitative NBT reduction and bactericidal capacity | Coautor: Armendares S., Kretschmer R.R., López-Osuna M., De La Rosa L. | 1974 | CLIN IMMUNOL IMMUNOP | WoS-id: A1974T462900001
Scopus-id: 2-s2.0-0016244579
| 30 | 23 |
| 79 | Histidinaemia in a consanguineous marriage | Coautor: Armendares S., Rostenberg I., Guizar J., Alejandre I., et al. | 1974 | JOURNAL OF MEDICAL GENETICS | WoS-id: A1974U364700016
Scopus-id: 2-s2.0-0016349618
| 2 | 1 |
| 80 | Genetic analysis of cleft lip with or without cleft palate and cleft palate alone in amexican group (author's transl) [Análisis genético de labio y paladar hendidos y paladar hendido solo. Estudio en una población mexicana] | 1ᵉʳ autor: Armendares S., Lisker R. | 1974 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1974U724900003
Scopus-id: 2-s2.0-18844474761
| 8 | 3 |
| 81 | Smith-Lemli-Opitz syndrome: description of 2 affected brothers, clinical characterization and hereditary mechanism [El sindrome de Smith-Lemli-Opitz: descripción de 2 hermanos afectados, caracterización clínica y mecanismo de transmisión | 1ᵉʳ autor: Armendares S., Carnevale A., Del Castillo V., Najar Aparicio A. | 1973 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1973Q109700002
Scopus-id: 2-s2.0-0015610573
| 7 | 4 |
| 82 | Somatometry of the face in preschool children. I. [SOMATOMETRIA DE CARA EN PREESCOLARES. I. EN LOS GRUPOS DE EDAD DE 5 Y 6 ANOS] | Coautor: Armendares S., Rostenberg I., Jimenez M., Daltabuit M. | 1973 | Archivos De Investigación Médica | WoS-id: A1973S127600001
Scopus-id: 2-s2.0-0015714235
| 1 | 0 |
| 83 | Harelip and cleft palate [EL LABIO Y PALADAR HENDIDOS] | 1ᵉʳ autor y autor de correspondencia: Armendares S. | 1973 | Bol.Med.Inst.Mex.Seguro Soc. | Scopus-id: 2-s2.0-0015760795
| 0 | 0 |
| 84 | Two male sibs with uterus and Fallopian tubes. A rare, probably inherited disorder | 1ᵉʳ autor: Armendares S., Buentello L., Frenk S. | 1973 | CLINICAL GENETICS | WoS-id: A1973Q118600021
Scopus-id: 2-s2.0-0015878261
| 30 | 21 |
| 85 | Familial Occurrence of Persistent Mullerian Structures in Otherwise Normal Males | Coautor: Armendares S., Brook C.G.D., Wagner H., Zachmann M., et al. | 1973 | British Medical Journal | WoS-id: A1973P235000011
Scopus-id: 2-s2.0-17544395820
| 106 | 92 |
| 86 | Differential diagnosis of congenital osteochondrodysplasia [Diagnóstico diferencial de las osteocondrodisplasias congénitas.] | Coautor y autor de correspondencia: Armendares S., Rostenberg I., Jiménez M. | 1973 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1973Q707100008
Scopus-id: 2-s2.0-18144449841
| 0 | 0 |
| 87 | Diastrophic dwarfism: apropos of a case [Enanismo diastrófico: a propósito de un caso.] | Coautor: Armendares S., Jiménez M., Rostenberg I., Manzano C., et al. | 1973 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1973Q707100006
Scopus-id: 2-s2.0-18144452438
| 0 | 0 |
| 88 | A dicentric Y chromosome without evidence of sex chromosomal mosaicism, 46,XYqdic, in a patient with features of Turner's syndrome. | 1ᵉʳ autor: Armendares S., Buentello L., Salamanca F., Cantu-Garza J.M. | 1972 | JOURNAL OF MEDICAL GENETICS | WoS-id: A1972M081700020
Scopus-id: 2-s2.0-0015314814
| 46 | 30 |
| 89 | Histopathologic study with cytogenetic correlation in 20 cases of gonadal dysgenesis. | 2ᵒ autor: Armendares S., Márquez-Monter H., Buentello L., Villegas J. | 1972 | AM J CLIN PATHOL | WoS-id: A1972M210800004
Scopus-id: 2-s2.0-0015321656
| 21 | 19 |
| 90 | Dermatoglyphics in Down's syndrome. Comparison of results with those of an urban Mexican population [Dermatoglífos en el sindrome de Down. Comparación de los resultados con los de una población mexicana urbana.] | 1ᵉʳ autor: Armendares S., Del Castillo V., Cantú J.M. | 1972 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1972N162600003
Scopus-id: 2-s2.0-0015327857
| 0 | 0 |
| 91 | Prenatal diagnosis of hereditary diseases. II. Risks and indications [Diagnóstico prenatal de enfermedades herditarias. II. Riesgos e indicationes.] | 1ᵉʳ autor y autor de correspondencia: Armendares S. | 1972 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0015385620
| 0 | 0 |
| 92 | Research priorities in genetics in Latin America [Prioridades de investigación en genética en Latinoamérica.] | 2ᵒ autor y autor de correspondencia: Armendares S., Lisker R. | 1972 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0015385817
| 0 | 0 |
| 93 | Ring D 1 chromosome with remarkable morphological variation in a boy with mental retardation. | Coautor y autor de correspondencia: Armendares S., Salamanca F., Buentello L. | 1972 | ANN GENET-PARIS | WoS-id: A1972N626600009
Scopus-id: 2-s2.0-0015390320
| 10 | 7 |
| 94 | GENETICA EN CIRUGIA | Coautor y autor de correspondencia: Armendares S., Shein M., German J. | 1972 | Rev.Cir.Hosp.Juarez | Scopus-id: 2-s2.0-0015437702
| 0 | 0 |
| 95 | Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome II. | 2ᵒ autor: Armendares S., Magenis R.E., Hecht F., Weleber R.G., et al. | 1972 | ANN GENET-PARIS | WoS-id: A1972O519500007
Scopus-id: 2-s2.0-0015451242
| 38 | 22 |
| 96 | Dermatoglyphics in Turner's syndrome (45,X). Comparison of results with those of a normal urban Mexican population [Dermatoglífos en el sindrome de Turner (45,X). Comparación de los resultados con los de una poblacion Mexicana urbana norma | 1ᵉʳ autor: Armendares S., Jiménez A.M., Cantú J.M. | 1972 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1972N162600004
Scopus-id: 2-s2.0-18244428207
| 3 | 2 |
| 97 | Noxious effects of various drugs and medicaments on the genetic material. II. The problem of lysergic acid diethylamide (LSD) [Efectos deletéreos de algunas drogas y medicamentos sobre el material genético. II. El problema de la diethilami | 1ᵉʳ autor y autor de correspondencia: Armendares S. | 1971 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0015023148
| 0 | 0 |
| 98 | Partial monosomy of a G group chromosome (45,XY,G-46,XY,Gr): report of a new case. | 1ᵉʳ autor: Armendares S., Buentello L., Cantu-Garza J.M. | 1971 | ANN GENET-PARIS | WoS-id: A1971J078900001
Scopus-id: 2-s2.0-0015030068
| 19 | 10 |
| 99 | Cp trisomy: a new syndrome [Trisomie Cp: un nouveau syndrome.] | Coautor y autor de correspondencia: Armendares S., Canu J.M., Buentello L. | 1971 | ANN GENET-PARIS | Scopus-id: 2-s2.0-0015122440
| 0 | 16 |
| 100 | An extra small metacentric autosome in a mentally retarded boy with multiple malformations. | 1ᵉʳ autor: Armendares S., Buentello L., Salamanca F. | 1971 | JOURNAL OF MEDICAL GENETICS | WoS-id: A1971K446000019
Scopus-id: 2-s2.0-0015123652
| 14 | 8 |
| 101 | 6-phosphogluconate dehydrogenase (6-P-GD) in Down's syndrome. | Coautor: Armendares S., Lisker R., Mora G., Buentello L. | 1971 | CLINICAL GENETICS | Scopus-id: 2-s2.0-0015187910
| 0 | 3 |
| 102 | Chromosome changes in megaloblastic anemia before and after treatment [Alteraciones cromosómicas en la anemia megaloblástica antes y después del tratamiento.] | Coautor y autor de correspondencia: Armendares S., Salamanca F., Arias y Arias J. | 1971 | Archivos De Investigación Médica | Scopus-id: 2-s2.0-0015193540
| 0 | 0 |
| 103 | Chromosome abnormalities in severe protein calorie malnutrition [20] | 1ᵉʳ autor: Armendares S., Salamanca F., Frenk S. | 1971 | Nature | WoS-id: A1971J850700042
Scopus-id: 2-s2.0-0015237314
| 61 | 53 |
| 104 | Dermatoglyphics in the Stein-Leventhal syndrome [Dermatoglifos en el síndrome de Stein-Leventhal.] | Coautor: Armendares S., Braxs J., Salamanca F., Buentello L., et al. | 1971 | Archivos De Investigación Médica | Scopus-id: 2-s2.0-18144447409
| 0 | 2 |
| 105 | Genetic factors that are involved in the growth and development of the child [Factores genéticos que intervienen en el crecimiento y desarrollo del niño.] | 1ᵉʳ autor y autor de correspondencia: Armendares S. | 1970 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0014771506
| 0 | 0 |
| 106 | Various epidemiological aspects of Down's syndrome [Algunos aspectos epidemiológicos del sindrome de Down.] | 1ᵉʳ autor y autor de correspondencia: Armendares S. | 1970 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0014777022
| 0 | 0 |
| 107 | Chromosome study in male prisoners in a Mexican penitentiary [Estudio cromosómico en prisioneros del sexo masculino en una penitenciaría Mexicana.] | 2ᵒ autor y autor de correspondencia: Armendares S., Buentello L. | 1970 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | Scopus-id: 2-s2.0-0014808955
| 0 | 2 |
| 108 | Familial extra centric bisatellited chromosome. | 1ᵉʳ autor: Armendares S., Buentello L., Cuevas-Sosa A., Cantú-Garza J.M. | 1969 | Cytogenetics | WoS-id: A1969D250900001
Scopus-id: 2-s2.0-0014450743
| 27 | 16 |
| 109 | Genetics in the practice of medicine. 3. Inheritance of congenital malformations [Génetica en la práctica médica. 3. Herencia de la malformaciones congénitas.] | 1ᵉʳ autor y autor de correspondencia: Armendares S. | 1969 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0014576001
| 0 | 0 |
| 110 | Cytogenetic aspects of the polycystic ovary syndrome. Review of the literature and presentation of 10 cases [Aspectos citogenéticos del síndrome de ovarios poliquisticos. Revisión de la literatura y presentación de 10 casos.] | 2ᵒ autor y autor de correspondencia: Armendares S., González González L. | 1968 | Ginecología Y Obstetricia De México | Scopus-id: 2-s2.0-0014261496
| 0 | 0 |
| 111 | Congenital heart diseases in chromosome abnormalities. I. In Down's syndrome (mongolism) [Cardiopatías congénitas en las anormalidades cromosómicas. I. En el síndrome de Down (mongolismo)] | 1ᵉʳ autor: Armendares S., Pérez Treviño C. | 1968 | Archivos Del Instituto De Cardiología De México | Scopus-id: 2-s2.0-0014350590
| 0 | 0 |
| 112 | Iliac Index in Newborns: Comparative Values at Term, in Prematurity, and in Down's Syndrome | 1ᵉʳ autor: Armendares S., Urrusti-Sanz J., Diaz-Del-Castillo E. | 1967 | American Journal Of Diseases Of Children | WoS-id: A19678943500009
Scopus-id: 2-s2.0-0014051414
| 8 | 6 |
| 113 | Genetics and pathology. 3. Chromosome abnormalities and disease [Genética y patológia. 3. Anormalidades cromosomicas y enfermedad.] | 1ᵉʳ autor y autor de correspondencia: Armendares S. | 1967 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0014162039
| 0 | 0 |
| 114 | SOMATIC GROWTH AND MENTAL DEVELOPMENT IN CHILDREN WITH CONGENITAL HYPOTHYROIDISM. [CRECIMIENTO SOM'ATICO Y DESARROLLO MENTAL EN NI NOS CON HIPOTIROIDISMO CONG'ENITO.] | 2ᵒ autor: ARMENDARES S., CHAVARRIA C., ANTHONY H., CRAVIOTO J., et al. | 1964 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | Scopus-id: 2-s2.0-75949151448
| 0 | 0 |
| 115 | Mental development of children with congenital hypothyroidism. | Coautor y autor de correspondencia: ARMENDARES S., ANTHONY E., FRENK S. | 1962 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-73649202571
| 0 | 0 |
| 116 | Somatic growth of cretinous children given substitute treatment | 2ᵒ autor: Armendares S., CHAVARRIA C., CRAVIOTO J. | 1962 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-84961061391
| 0 | 0 |
ID's SCOPUS