G. Pérez-García

[Implications in primary health care of medical genetics and genomic in type 2 diabetes mellitus].

N. Villa‐Ruano, C. Cabrera-Pivaral, S. Ramirez-Garcia, 2013, Revista medica del Instituto Mexicano del Seguro Social.

Clinical and molecular analysis in a series of Mexican patients with clinical diagnosis of Fibrodysplasia Ossificans Progressiva (FOP)

L. E. Martínez-de-Villarreal, L. Taja-Chayeb, L. D. Campos-Acevedo, 2016 .

Clinical, Cytogenetic, Environmental and Inheritance Findings in Mexican Neonates with VACTERL Association

G. Pérez-García, V. M. Salinas-Torres, Nicolás Pérez-García, 2014, The Indian Journal of Pediatrics.

Genomic Characterization of a Rare, de Novo Unbalanced ins(3;1)(p25.3;q21.3q23.3) in a Female Child with Multiple Congenital Anomalies

C. D. Robles-Espinoza, C. Córdova-Fletes, C. Castañeda-García, 2020, Cytogenetic and Genome Research.

Transverse meromelia in all four limbs with characteristic facie associated with cocaine abuse in the first trimester of pregnancy

A. Raya-Trigueros, G. Pérez-García, J. A. Gutiérrez-Padilla, 2012 .

The 22q distal trisomy syndrome in a recombinant child.

G. Pérez-García, R. Martínez y Martínez, H. Rivera, 1988, Annales de genetique.

A further whole arm 1;19 translocation with alpha-satellite DNA breakage.

H. Rivera, P. Malet, G. Pérez-García, 1997, Genetic counseling.

Bilateral tibial hemimelia type 1 (1a and 1b) with T9 and T10 hemivertebrae: a novel association.

G. Pérez-García, V. M. Salinas-Torres, Nicolás Pérez-García, 2013, Sao Paulo medical journal = Revista paulista de medicina.

Choreoacanthocytosis in a Mexican family.

A. Monaco, C. Dobson-Stone, E. Chiquete, 2007, Archives of neurology.

MRI findings in SANDO variety of the ataxia-neuropathy spectrum with a novel mutation in POLG (c.3287G>T): A case report

J. Ruiz-Sandoval, J. D. Parada-Garza, G. Pérez-García, 2020, Neuromuscular Disorders.