R. García-Cavazos

Genetic aspects in the medical approach of congenital heart defects

G. Queipo, F. Coronel-Cruz, A. Cervantes, 2020, Revista M�dica del Hospital General de M�xico.

Carrier detection and prenatal molecular diagnosis in a Duchenne muscular dystrophy family without any affected relative available.

L. Orozco, A. Carnevale, A. González-del Angel, 2001, Annales de genetique.

[Skin and tissue bank: Operational model for the recovery and preservation of tissues and skin allografts].

C. Machuca-Rodríguez, R. García-Cavazos, Francisco Martínez-Flores, 2016, Cirugia y cirujanos.

Molecular screening of the CFTR gene in Mexican patients with congenital absence of the vas deferens.

L. Orozco, A. Carnevale, S. Jiménez-Morales, 2012, Genetic testing and molecular biomarkers.

45,X/47,XXX/47,XX, del(Y)(p?)/46,XX mosaicism causing true hermaphroditism

G. Queipo, Í. Palma, Rocío Peña, 2004, American journal of medical genetics. Part A.

Mosaicism Causing True Hermaphroditism

G. Queipo, Í. Palma, Rocío Peña, 2004 .

A case of mosaic Down's syndrome with two Robertsonian translocations.

E. Cortés-Gutiérrez, R. García-Cavazos, C. Leal-Garza, 1996, Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion.

Inside the Outbreak of the 2009 Influenza A (H1N1)v Virus in Mexico

E. Lara-Padilla, Luis M. Teran, A. Domínguez-López, 2010, PloS one.

Effect on risk of anencephaly of gene–nutrient interactions between methylenetetrahydrofolate reductase C677T polymorphism and maternal folate, vitamin B12 and homocysteine profile

V. Borja-Aburto, M. Rodríguez-Barranco, M. Lacasaña, 2012, Public Health Nutrition.

Identification of influenza A pandemic (H1N1) 2009 variants during the first 2009 influenza outbreak in Mexico City.

E. Lara-Padilla, C. Garibay-Orijel, A. Domínguez-López, 2010, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

Identification of drugs as regulators on the activity of Egr-1 promoter in human fibroblasts transduced with AdΔegr-1-Luc 7 Identificación de fármacos reguladores de la actividad del promotor Egr-1 en fibroblastos humanos transducidos con AdΔegr-1-Luc 7

F. A. Jiménez-Orozco, M. Valdés-Flores, R. García-Cavazos, 2019 .

Prenatal diagnosis in a cystic fibrosis family: a combined molecular strategy for a precise diagnosis.

L. Orozco, M. Chávez-Saldaña, R. M. Vigueras, 2011, Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion.

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

H. Rangel-Villalobos, E. Arámbula-Meraz, C. Galaviz-Hernández, 2012, Revista espanola de cardiologia.