Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH

We present prenatal diagnosis of a case with a rare de novo interstitial deletion of 1q21‐q25.1 by oligo array CGH and provide detailed information on unbalanced gene content and the breakpoints. The affected fetus was delivered at 37 weeks’ gestation with a unique clinical phenotype.

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Detalhes bibliográficos
Publicado no:Clin Case Rep
Main Authors: Shariati, Gholamreza, Saberi, Alihossein, Hamid, Mohammad, Galehdari, Hamid, Sedaghat, Alireza, Abdorasuli, Nehzat
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2018
Assuntos:
Case Reports
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6099003/
https://ncbi.nlm.nih.gov/pubmed/30147883
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.1604
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