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Archivos De La Sociedad Espanola De Oftalmologia|October 13, 2012
[Ophthalmic manifestations in Mexican patients with Fabry disease]K J Beltrán-Becerra, B E Ríos-González, B E Gutiérrez-Amavizca, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 7, 2020
Generalized hypertrichosis syndromes in MexicoThania Alejandra Aguayo-Orozco, Blanca Estela Ríos-González, Anna Gabriela Castro-Martínez, et al.
European Review for Medical and Pharmacological Sciences|August 9, 2020
The rs2234694 and 50 bp Insertion/Deletion polymorphisms of the SOD1 gene are associated with breast cancer risk in a Mexican populationM P Gallegos-Arreola, M A Ramírez-Hernández, L E Figuera, et al.
Gynecologic and Obstetric Investigation|February 23, 2012
The TP53 16-bp duplication polymorphism is enriched in endometriosis patientsM P Gallegos-Arreola, L E Valencia-Rodríguez, A M Puebla-Pérez, et al.
Genetics and Molecular Research : GMR|November 5, 2016
eNOS gene Glu298Asp and 4b/a polymorphisms are associated with renal function parameters in Mexican patients with Fabry diseaseA Marin-Medina, A J L Brambila-Tapia, V J Picos-Cárdenas, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 25, 2025
Clinical ManifestationsAngélica Zuno-Reyes, Karina Pérez-Rubio, Ricardo Jáuregui Torres, et al.
Genetics and Molecular Research : GMR|May 20, 2017
Determination of SCN1A genetic variants in Mexican patients with refractory epilepsy and Dravet syndromeR E Jiménez-Arredondo, A J L Brambila-Tapia, F M Mercado-Silva, et al.
American Journal of Medical Genetics|March 17, 1997
Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: further delineation of a new genetic syndromeD Garcia-Cruz, J Sánchez-Corona, Z Nazará, et al.
American Journal of Human Genetics|May 1, 1997
Molecular analysis of deletion (17)(p11.2p11.2) in a family segregating a 17p paracentric inversion: implications for carriers of paracentric inversionsS P Yang, S I Bidichandani, L E Figuera, et al.
Genetics and Molecular Research : GMR|November 14, 2013
Genetic contribution of CYP2C9, CYP2C19, and APOE variants in acenocoumarol responseJ A Nastasi-Catanese, J R Padilla-Gutiérrez, Y Valle, et al.
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