Microdeletion and Microduplication Analysis of Chinese Conotruncal Defects Patients with Targeted Array Comparative Genomic Hybridization

OBJECTIVE: The current study aimed to develop a reliable targeted array comparative genomic hybridization (aCGH) to detect microdeletions and microduplications in congenital conotruncal defects (CTDs), especially on 22q11.2 region, and for some other chromosomal aberrations, such as 5p15-5p, 7q11.23...

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Detalles Bibliográficos
Autores principales: Gong, Xiaohui, Wu, Xi, Ma, Xiaojing, Wu, Dandan, Zhang, Ting, He, Li, Qin, Shengying, Li, Xiaotian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3788710/
https://www.ncbi.nlm.nih.gov/pubmed/24098474
http://dx.doi.org/10.1371/journal.pone.0076314

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3788710/
https://www.ncbi.nlm.nih.gov/pubmed/24098474
http://dx.doi.org/10.1371/journal.pone.0076314

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