C. Molina-Garay

Non-functional alternative splicing caused by a Latino pathogenic variant in a case of PMM2-CDG

H. Mora-Montes, C. E. Villarroel, R. Salinas-Marín, 2021, Molecular genetics and metabolism reports.

Identification through exome sequencing of the first PMM2-CDG individual of Mexican mestizo origin

R. Salinas-Marín, I. Martínez-Duncker, C.A. González-Domínguez, 2020, Molecular genetics and metabolism reports.

Clinical and genetic description of patients with prenatally identified cardiac tumors

C. Molina-Garay, K. Carrillo-Sánchez, M. Jiménez-Olivares, 2019, Prenatal diagnosis.

Clinical Manifestations, Mutational Analysis, and Immunological Phenotype in Patients with RAG1/2 Mutations: First Cases Series from Mexico and Description of Two Novel Mutations

L. Notarangelo, S. Rosenzweig, N. Pastor, 2021, Journal of Clinical Immunology.

ALG1-CDG Caused by Non-functional Alternative Splicing Involving a Novel Pathogenic Complex Allele

H. Freeze, M. He, H. Mora-Montes, 2021, Frontiers in Genetics.

Uterus infantilis: a novel phenotype associated with AARS2 new genetic variants. A case report

E. García-Latorre, I. Martínez-Duncker, E. S. Vargas-Cañas, 2023, Frontiers in Neurology.

Corrigendum: ALG1-CDG Caused by Non-Functional Alternative Splicing Involving a Novel Pathogenic Complex Allele

H. Freeze, H. Mora-Montes, K. Raymond, 2021, Frontiers in Genetics.

IKZF1plus is a frequent biomarker of adverse prognosis in Mexican pediatric patients with B-acute lymphoblastic leukemia

J. Mejía-Aranguré, E. Mendoza-Caamal, S. Jiménez-Morales, 2024, Frontiers in oncology.