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Alicia Cervantes

National Autonomous University of Mexico
Hospital General de México

31

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320

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Mosaic proximal trisomy 13q and regular trisomy 13 in a female patient with long survival: Involvement of an incomplete trisomic rescue and a chromothripsis event.

2021 Molecular Genetics & Genomic Medicine
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X-linked hypohidrotic ectodermal dysplasia by a de novo recurrent variant in a Mexican patient.

2020 Boletín médico del Hospital Infantil de México
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High penetrance of EDA pathogenic variants in Mexican female carriers with hypohidrotic ectodermal dysplasia

2020 Dermatologica Sinica
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Genetic aspects in the medical approach of congenital heart defects

2020
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Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population

2019 Annals of Hepatology
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Liver disease in pregnancy: Medical aspects and their implications for mother and child

2019 Annals of Hepatology
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Monosomy 9p24 in two non-related patients as result of a translocation (2;9).

2018 Archivos Argentinos De Pediatria
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Monosomía 9p24 secundaria a translocación (2;9) en dos pacientes no relacionadas.

2018 Archivos Argentinos De Pediatria
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Nance–Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature

2018 Ophthalmic Genetics
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Mutational spectrum of EDA and EDAR genes in a cohort of Mexican mestizo patients with hypohidrotic ectodermal dysplasia

2017 Journal of The European Academy of Dermatology and Venereology
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Citations (3)