Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Mario Rodríguez-Camacho

2PUBLICATIONS

8CO-AUTHORS

English languageDevelopmental genetics (incl. sex determination)

Featured researcher

Get your video featured.

Publish with JoVE

Featured researcher

Get your video featured.

Publish with JoVE

Publications (2)

Sort by Publication Date:

|Sep 08, 2025

Cognitive deficits in Spanish-speaking Mexican children with developmental dyslexia.

José-Ángel Cabañas-Tinajero, Belén Prieto-Corona, Mario Rodríguez-Camacho

|Dec 15, 2022

Neuropsychological Genotype-Phenotype in Patients with Williams Syndrome with Atypical Deletions: A Systematic Review.

Carlos Alberto Serrano-Juárez, Belén Prieto-Corona, Mario Rodríguez-Camacho

Pageof 1

Frequent Collaborators

2 joint publications

Belén Prieto-Corona

2 joint publications

Ma Guillermina Yáñez-Téllez

1 joint publications

Carlos Alberto Serrano-Juárez

1 joint publications

Lucero Sandoval-Lira

1 joint publications

Ángel Fernando Villalva-Sánchez

1 joint publications

José-Ángel Cabañas-Tinajero

1 joint publications

Rosa Del Carmen Flores-Macías

1 joint publications

Josefina Ricardo-Garcell

Frequent Collaborators

2 joint publications

Belén Prieto-Corona

2 joint publications

Ma Guillermina Yáñez-Téllez

1 joint publications

Carlos Alberto Serrano-Juárez

1 joint publications

Lucero Sandoval-Lira

Top Related Videos

Advancing Dyslexia Assessment in Children Through Computerized Testing

Advancing Dyslexia Assessment in Children Through Computerized Testing

Published on : Aug 16, 2024

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on : Dec 01, 2017

See more related videos

Top Related Videos

Advancing Dyslexia Assessment in Children Through Computerized Testing

Advancing Dyslexia Assessment in Children Through Computerized Testing

Published on : Aug 16, 2024

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on : Dec 01, 2017

See more related videos