The Identification of Microdeletion and Reciprocal Microduplication in 22q11.2 Using High-Resolution CMA Technology

The chromosome 22q11.2 region has long been implicated in genomic diseases. Some genomic regions exhibit numerous low copy repeats with high identity in which they provide increased genomic instability and mediate deletions and duplications in many disorders. DiGeorge Syndrome is the most common del...

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Detalles Bibliográficos
Autores principales: Leite, Ana Julia Cunha, Pinto, Irene Plaza, Cunha, Damiana Mirian da Cruz e, Ribeiro, Cristiano Luiz, da Silva, Claudio Carlos, da Cruz, Aparecido Divino, Minasi, Lysa Bernardes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830712/
https://www.ncbi.nlm.nih.gov/pubmed/27123452
http://dx.doi.org/10.1155/2016/7415438

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830712/
https://www.ncbi.nlm.nih.gov/pubmed/27123452
http://dx.doi.org/10.1155/2016/7415438

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