Lista de obras -

Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly).

artículo científico publicado en 2000

Clinical delineation of a patient with trisomy 1q32.qter and monosomy 5p resulting from a familial translocation 1;5

scientific article published on 01 January 2010

Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome.

artículo científico publicado en 2013

Diabetes and obesity during pregnancy are associated with oxidative stress genotoxicity in newborns

scientific article published on 01 April 2019

Genetic polymorphisms associated with pediatric-onset type 2 diabetes: A family-based transmission disequilibrium test and case-control study

scientific article published on 06 February 2019

Gestational diabetes mellitus and congenital malformations

artículo científico publicado en 2001

Maternal Obesity as a Risk Factor for the Development of Total Anomalous Pulmonary Venous Connection in Their Offspring

scientific article published on 01 February 2018

Maternal obesity increases oxidative stress in the newborn

artículo científico publicado en 2015

Methylenetetrahydrofolate reductase gene 677CT polymorphism and isolated congenital heart disease in a Mexican population.

artículo científico publicado en 2011

MicroRNAs Association in the Cardiac Hypertrophy Secondary to Complex Congenital Heart Disease in Children.

artículo científico publicado en 2017

Microdeletion 22q11.2 syndrome: Does thymus incidental surgical resection affect its immunological profile?

artículo científico publicado en 2018

Mouse models for the study of postnatal cardiac hypertrophy.

artículo científico publicado en 2015

Ontogeny of the facial phenotypic variability in Mexican patients with 22q11.2 deletion syndrome

scientific article published on 11 December 2019

Polymorphism 677C → T MTHFR gene in Mexican mothers of children with complex congenital heart disease.

artículo científico publicado en 2012

Prevalence and spectrum of diseases that predispose to sudden cardiac death in Mexican children: a sample obtained from The Federico Gomez Children's Hospital of Mexico

artículo científico publicado en 2017

Velocardiofacial syndrome in Mexican patients: Unusually high prevalence of congenital heart disease.

artículo científico publicado en 2015

Lista de obras de

Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly).

Clinical delineation of a patient with trisomy 1q32.qter and monosomy 5p resulting from a familial translocation 1;5

Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome.

Diabetes and obesity during pregnancy are associated with oxidative stress genotoxicity in newborns

Genetic polymorphisms associated with pediatric-onset type 2 diabetes: A family-based transmission disequilibrium test and case-control study

Gestational diabetes mellitus and congenital malformations

Maternal Obesity as a Risk Factor for the Development of Total Anomalous Pulmonary Venous Connection in Their Offspring

Maternal obesity increases oxidative stress in the newborn

Methylenetetrahydrofolate reductase gene 677CT polymorphism and isolated congenital heart disease in a Mexican population.

MicroRNAs Association in the Cardiac Hypertrophy Secondary to Complex Congenital Heart Disease in Children.

Microdeletion 22q11.2 syndrome: Does thymus incidental surgical resection affect its immunological profile?

Mouse models for the study of postnatal cardiac hypertrophy.

Ontogeny of the facial phenotypic variability in Mexican patients with 22q11.2 deletion syndrome

Polymorphism 677C → T MTHFR gene in Mexican mothers of children with complex congenital heart disease.

Prevalence and spectrum of diseases that predispose to sudden cardiac death in Mexican children: a sample obtained from The Federico Gomez Children's Hospital of Mexico

Velocardiofacial syndrome in Mexican patients: Unusually high prevalence of congenital heart disease.