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A report on seven fetal cases associated with 15q11‐q13 microdeletion and microduplication

Abstract Background The 15q11‐q13 region contains three breakpoints (BP1 to BP3), and copy number variations often occur in the region. Aims 15q11‐q13 microdeletion and microduplication are usually associated with Prader‐Willi and Angelman syndromes, respectively. It is not yet clear to what extent...

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Hoofdauteurs: Xiuzhu Huang, Jieping Chen, Wenlong Hu, Lu Li, Huiyan He, Hui Guo, Qiuyan Liao, Mei Ye, Donge Tang, Yong Dai
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Wiley 2021-03-01
Reeks:Molecular Genetics & Genomic Medicine
Onderwerpen:
15q11‐q13
Angelman syndrome
microdeletion
microduplication
Prader‐Willi syndrome
Online toegang:https://doi.org/10.1002/mgg3.1605
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