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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Publicat a:Biomed Res Int
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Hindawi Publishing Corporation 2016
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4830712/
https://ncbi.nlm.nih.gov/pubmed/27123452
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/7415438
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