22q11.2 deletion detected by in situ hybridization in Mexican patients with velocardiofacial syndrome-like features

INTRODUCTION: Deletion 22q11.2 occurs in 1:4,000-1:6,000 live births while 10p13p14 deletion is found in 1:200,000 newborns. Both deletions have similar clinical features such as congenital heart disease and immunological anomalies. OBJECTIVE: We looked for a 22q11.2 deletion in Mexican patients wit...

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Detalles Bibliográficos
Autores principales: Ramírez-Velazco, Azubel, Rivera, Horacio, Vásquez-Velázquez, Ana Isabel, Aguayo-Orozco, Thania Alejandra, Delgadillo-Pérez, Saturnino, Domínguez, Maria Guadalupe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Universidad del Valle 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220481/
https://www.ncbi.nlm.nih.gov/pubmed/30410196
http://dx.doi.org/10.25100/cm.v49i2.3402

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