Juan C. Montiel-Huicochea
Seguro Social, MEX, Mexico
Last Updated: 09/26/2026
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Found 9 publications
Clinical and molecular characterization of six Mexican patients with FGFR2-related syndromic craniosynostosis.
Journal: Gaceta medica de Mexico
Published: January 01, 2025
Cytogenomic description of a Mexican cohort with differences in sex development.
Journal: Molecular cytogenetics
Published: February 16, 2024
Clustering of Genetic Anomalies of Cilia Outer Dynein Arm and Central Apparatus in Patients with Transposition of the Great Arteries.
Journal: Genes
Published: August 11, 2022
Clinical, radiological, and molecular diagnosis of progressive fibrodysplasia ossificans.
Journal: Boletin medico del Hospital Infantil de Mexico
Published: May 03, 2021
Identification of genomic copy number variations in lung benign metastasizing leiomyomatosis.
Journal: The clinical respiratory journal
Published: June 20, 2018
Insights about uncertainty in genetic counseling
Journal: Revista medica del Instituto Mexicano del Seguro Social
Published: October 29, 2015
Clinical and molecular characterization of a patient with 15q21.2q22.2 deletion syndrome.
Journal: Cytogenetic and genome research
Published: October 17, 2014
The role of the medical geneticist in the pediatric consultation
Journal: Revista medica del Instituto Mexicano del Seguro Social
Published: July 02, 2014
Duplication of the Miller-Dieker Critical Region in a Patient with a Subtelomeric Unbalanced Translocation t(10;17)(p15.3;p13.3).
Journal: Molecular syndromology
Published: May 14, 2012
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Last Updated: 09/26/2026