Analysis of copy number variations of WNT4 gene in a Chinese population with Müllerian anomalies

BACKGROUND: To investigate the genetic contribution of copy number variations (CNVs) in Wingless-type MMTV integration site family, member 4 (WNT4), in a Chinese population with Müllerian anomalies (MA), copy number analysis of WNT4 by Multiplex ligation‐dependent probe amplification (MLPA) was perf...

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Gepubliceerd in:Orphanet J Rare Dis
Hoofdauteurs: Zhu, Ying, Wang, Ruyi, Cheng, Yun, Han, Yang, Li, Tengyan, Cao, Yunxia, Wang, Binbin
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2021
Onderwerpen:
Research
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8183036/
https://ncbi.nlm.nih.gov/pubmed/34099025
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-021-01888-0
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