G. Pacheco-Cuéllar

A Novel PGM3 Mutation Is Associated With a Severe Phenotype of Bone Marrow Failure, Severe Combined Immunodeficiency, Skeletal Dysplasia, and Congenital Malformations

E. Haddad, V. Désilets, Philippe M. Campeau, 2017, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Asociación de los polimorfismos del gen ADRB1 y la respuesta hipotensora ocular al betaxolol tópico Association of polymorphisms of gene ADRB1 and the ocular hypotensi- ve response to topic betaxolol

L. González-Huerta, S. Cuevas-Covarrubias, G. Pacheco-Cuéllar, 2012 .

Noonan syndrome: Prenatal diagnosis in a woman carrying a PTPN11 gene mutation

A. Pérez-Cabrera, L. González-Huerta, S. Cuevas-Covarrubias, 2010, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.