Villarroel Camilo E - Department of Human Genetics, National Institute of Pediatrics

C. A. Gonzalez-Dominguez,C. E. Villarroel,M. Rodriguez-Morales, S. Manrique-Hernandez, A. Gonzalez-Jaimes, F. Olvera-Rodriguez, K. Beutelspacher, C. Molina-Garay, K. Carrillo-Sanchez, L. L. Flores-Lagunes, M. Jimenez-Olivares, A. Munoz-Rivas, M. E. Cruz-Munoz,H. M. Mora-Montes,R. Salinas-Marin,C. Alaez-Verson,I Martinez-Duncker

Molecular genetics and metabolism reports（2021）

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Previously Undescribed Phenotypic Findings and Novel ACTG1 Gene Pathogenic Variants in Baraitser-Winter Cerebrofrontofacial Syndrome

Oscar F. Chacon-Camacho,Tania Barragan-Arevalo,Camilo E. Villarroel,Monica Almanza-Monterrubio,Juan Carlos Zenteno

European journal of medical genetics（2020）

Cited5Views0WOSBibtex

Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review

Yokoyama Emiy,Villarroel Camilo E., Diaz Sinhué,Del Castillo Victoria,Pérez-Vera Patricia,Salas Consuelo, Gómez Samuel, Barreda Reneé,Molina Bertha, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México

Molecular Cytogenetics（2020）

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