Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array

The q11.2 region on chromosome 22 contains numerous low-copy repeats that lead to deleted or duplicated regions in the chromosome, thereby resulting in different syndromes characterized by intellectual disabilities or congenital anomalies. The association between patient phenotypes and 22q11.2 copy...

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Bibliografiska uppgifter
I publikationen:Mol Biol Rep
Huvudupphovsmän: Cai, Meiying, Lin, Na, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Li, Ying, Lin, Yuan, Huang, Hailong, Xu, Liangpu
Materialtyp: Artigo
Språk:Inglês
Publicerad: Springer Netherlands 2020
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Original Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC7588391/
https://ncbi.nlm.nih.gov/pubmed/32935260
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11033-020-05815-7
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