L. Márquez-Quiróz

UPD(14)mat and UPD(14)mat in concomitance with mosaic small supernumerary marker chromosome 14 in two new patients with Temple syndrome.

C. E. Villarroel, P. Pérez-Vera, C. Salas-Labadía, 2021, European Journal of Medical Genetics.

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

P. Medina-Bravo, N. Garibay-Nieto, R. Sánchez-Urbina, 2015, International journal of pediatric otorhinolaryngology.

Oropharyngeal dysphagia in early stages of myotonic dystrophy type 1

B. Cisneros, H. Cortés, J. Magaña, 2019, Muscle & nerve.

Cognitive Decline and White Matter Integrity Degradation in Myotonic Dystrophy Type I

R. Díaz, L. Beltrán-Parrazal, C. Hernandez-Castillo, 2020, Journal of neuroimaging : official journal of the American Society of Neuroimaging.

Origin of the myotonic dystrophy type 1 mutation in Mexican population and influence of Amerindian ancestry on CTG repeat allelic distribution

O. Hernández-Hernández, E. Mendoza-Caamal, Y. Tapia-Guerrero, 2017, Neuromuscular Disorders.