| 1 | Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review | Coautor: Cervantes-Barragan, D., Martinez-Hernandez, A., Martinez-Anaya, D., Duran-McKinster, C., et al. | 2022 | BMC MEDICAL GENOMICS | WoS-id: 000877014900002
Scopus-id: 2-s2.0-85140943693
| 0 | 0 |
| 2 | Genetic and clinical characterization of 73 Pigmentary Mosaicism patients: Revealing the genetic basis of clinical manifestations | Coautor: Cervantes-Barragan, D., Salas-Labadia, C., Gomez-Carmona, S., Cruz-Alcivar, R., et al. | 2019 | ORPHANET JOURNAL OF RARE DISEASES | WoS-id: 000497424400002
Scopus-id: 2-s2.0-85075037719
| 17 | 19 |
| 3 | Genomic chaos in peripheral blood lymphocytes of Hodgkin's lymphoma patients one year after ABVD chemotherapy/radiotherapy | Coautor: Cervantes-Barragan, David E., Ramos, Sandra, Navarrete-Meneses, Pilar, Molina, Bertha, et al. | 2018 | ENVIRONMENTAL AND MOLECULAR MUTAGENESIS | WoS-id: 000447275100008
Scopus-id: 2-s2.0-85052954475
| 12 | 15 |
| 4 | Newborn screening for six lysosomal storage disorders in a cohort of Mexican patients: Three-year findings from a screening program in a closed Mexican health system | Coautor: Cervantes-Barragán D.E., Navarrete-Martínez J.I., Limón-Rojas A.E., Gaytán-García M.D.J., et al. | 2017 | MOLECULAR GENETICS AND METABOLISM | WoS-id: 000402024100003
Scopus-id: 2-s2.0-85019056946
| 41 | 46 |
| 5 | Clinical heterogeneity in Andersen-Tawil syndrome | Coautor y autor de correspondencia: Cervantes-Barragan D.E., Totomoch-Serra A., Márquez M.F. | 2017 | NEUROMUSCULAR DISORDERS | WoS-id: 000416197000013
Scopus-id: 2-s2.0-85030673026
| 2 | 2 |
| 6 | Sanger sequencing as a first-line approach for molecular diagnosis of Andersen-Tawil syndrome | Coautor y autor de correspondencia: Cervantes-Barragán D.E., Marquez M.F., Totomoch-Serra A. | 2017 | F1000 Research | Scopus-id: 2-s2.0-85031004381
| 0 | 27 |
| 7 | Cytogenomic and phenotypic analysis in low-level monosomy 7 mosaicism with non-supernumerary ring chromosome 7 | 2ᵒ autor: Cervantes-Barragán D.E., Salas-Labadía C., Cruz-Alcívar R., Daber R.D., et al. | 2014 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000337633300023
Scopus-id: 2-s2.0-84902548321
| 7 | 7 |
| 8 | Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome | Coautor: Cervantes-Barragán D.E., Nakamura K., Kato M., Osaka H., et al. | 2013 | Neurology | WoS-id: 000330767700014
Scopus-id: 2-s2.0-84884572095
| 169 | 186 |
| 9 | Setleis syndrome in Mexican-Nahua sibs due to a homozygous TWIST2 frameshift mutation and partial expression in heterozygotes: Review of the focal facial dermal dysplasias and subtype reclassification | 1ᵉʳ autor: Cervantes-Barragán D.E., Villarroel C.E., Medrano-Hernández A., Durán-McKinster C., et al. | 2011 | JOURNAL OF MEDICAL GENETICS | Scopus-id: 2-s2.0-80955136596
| 0 | 27 |
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