David E. Cervantes‐Barragán

Clinical spectrum of <i>SCN2A</i> mutations expanding to Ohtahara syndrome

Kazuyuki Nakamura, Mitsuhiro Kato, Hitoshi Osaka et al. · Neurology · 2013 · 196 citations

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

Juana Inés Navarrete‐Martínez, Ana Elena Limón-Rojas, Maria de Jesús Gaytán-García et al. · Molecular Genetics and Metabolism · 2017 · 57 citations

Early Diagnosis, Three-year Findings, Neonatology +8

Sanger sequencing as a first-line approach for molecular diagnosis of Andersen-Tawil syndrome

Armando Totomoch-Serra, Manlio F. Márquez, David E. Cervantes‐Barragán · F1000Research · 2017 · 33 citations · Full text

Setleis syndrome in Mexican-Nahua sibs due to a homozygous <i>TWIST2</i> frameshift mutation and partial expression in heterozygotes: review of the focal facial dermal dysplasias and subtype reclassification

David E. Cervantes‐Barragán, Camilo E. Villarroel, A. Medrano-Hernandez et al. · Journal of Medical Genetics · 2011 · 30 citations

Genetic and clinical characterization of 73 Pigmentary Mosaicism patients: revealing the genetic basis of clinical manifestations

Consuelo Salas‐Labadía, Samuel Gómez-Carmona, Roberto Cruz‐Alcívar et al. · Orphanet Journal of Rare Diseases · 2019 · 22 citations · Full text