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Sergio A. Cuevas-Covarrubias

Hospital General de México

63

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415

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Characterization of two children with tetrasomy 18p syndrome through multiplex ligation-dependent probe amplification and single nucleotide polymorphism-array: expanding phenotype?

2021
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Naltrexone, a therapeutic alternative in Darier disease

2021
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Expression of metalloproteinases MMP-2 and MMP-9 is associated to the presence of androgen receptor in epithelial ovarian tumors

2020 Journal of Ovarian Research
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Submicroscopic 11p13 deletion including the elongator acetyltransferase complex subunit 4 gene in a girl with language failure, intellectual disability and congenital malformations: A case report

2020 World Journal of Clinical Cases
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Whole sequence of the mitochondrial DNA genome of Kearns Sayre Syndrome patients: Identification of deletions and variants

2019 Gene
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Gender-specific differences in clinical and metabolic variables associated with NAFLD in a Mexican pediatric population

2019 Annals of Hepatology
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Molecular characterization of Axenfeld-Rieger spectrum and other anterior segment dysgeneses in a sample of Mexican patients

2018 Ophthalmic Genetics
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A case report of a patient with mucopolysaccharidosis type II

2017 Revista Médica del Hospital General de México
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Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis

2017 Molecular Syndromology
- Olga Messina-Baas
- Sergio A. Cuevas-Covarrubias
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Duo test and aneuploidy detection in women under 35 years of age with high-risk pregnancy at the Hospital General de México

2017 Revista Médica del Hospital General de México
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