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Publications by F. Martínez-Hernández

Mutations in the FGFR2 Gene in Mexican Patients With Apert Syndrome

Genetics and Molecular Research

Molecular Biology

English

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Apert Syndrome With FGFR2 758 C > G Mutation: A Chinese Case Report

Frontiers in Genetics

Molecular Medicine

English

The Study of Abnormal Bone Development in the Apert Syndrome Fgfr2+/S252w Mouse Using a 3D Hydrogel Culture Model

English

Presence of the Apert Canonical S252W FGFR2 Mutation in a Patient Without Severe Syndactyly.

Journal of Medical Genetics

English

Novel GRN Mutations in Patients With Corticobasal Syndrome

Scientific Reports

Multidisciplinary

English

Mutations in the Nijmegen Breakage Syndrome Gene in Medulloblastomas

Clinical Cancer Research

Cancer Research

English

Mutations of the GLA Gene in Young Patients With Stroke

Cardiovascular Medicine

Specialized Nursing

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Investigating the Effects of Missense Mutations in MSH2 Gene Associated With Lynch Syndrome

Biophysical Journal

English

Novel Mutations in the IRF6 Gene in Brazilian Families With Van Der Woude Syndrome

International Journal of Molecular Medicine

English

Four Novel Thymidine Phosphorylase Gene Mutations in Mitochondrial Neurogastrointestinal Encephalomyopathy Syndrome (MNGIE) Patients

European Journal of Human Genetics

English