G. Castañeda-Cisneros

Autosomal dominant leukodystrophy presenting as Alzheimer's-type dementia.

Mariana Aurora Cansino-Torres, Valeria Sandoval-Rodríguez, M. Sáenz-Farret, 2017, Multiple sclerosis and related disorders.

Genetic approach in amyotrophic lateral sclerosis.

S. Ramirez-Garcia, D. García-Cruz, L. M. Baltazar-Rodríguez, 2020, Gaceta medica de Mexico.

A missense mutation, p.V132G, in the X‐linked spermine synthase gene (SMS) causes Snyder–Robinson syndrome

J. Śanchez-Corona, J. García-Ortiz, D E McCloskey, 2009, American journal of medical genetics. Part A.

Severe Craniofacial Involvement due to Amniotic Band Sequence

J. García-Ortiz, J. Nastasi-Catanese, E. López-Muñoz, 2018, Fetal and pediatric pathology.

Hemimegalencephaly with Facial Congenital Infiltrating Lipomatosis in a Child

J. Śanchez-Corona, Felipe Farías-Serratos, G. Castañeda-Cisneros, 2014, Iranian journal of public health.

A clinical report of the massive CAG repeat expansion in spinocerebellar ataxia type 2: Severe onset in a Mexican child and review previous cases

V. Volpini, J. García-Ortiz, S. Ramirez-Garcia, 2020, Genetics and molecular biology.

Constitutional duplication 11q23 de novo involving the MLL gene.

M. Partida-Pérez, M. G. López-Cardona, J. Śanchez-Corona, 2006, Genetic counseling.

Metaphyseal chondrodysplasia, upper limb mesomelia and normal height (mesomelic dysplasia camera type): Second report in a Mexican patient

J. Śanchez-Corona, J. García-Ortiz, R. Bañuelos-Acosta, 2008, American journal of medical genetics. Part A.

Cantu syndrome and lymphoedema

J. Śanchez-Corona, J. Cantú, S. Ramirez-Garcia, 2011, Clinical dysmorphology.

A familial case of Cantu craniofaciofronto digital syndrome

J. Śanchez-Corona, J. García-Ortiz, D. García-Cruz, 2012, Clinical dysmorphology.