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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Bibliographische Detailangaben
Veröffentlicht in:Clin Case Rep
Hauptverfasser: Shariati, Gholamreza, Saberi, Alihossein, Hamid, Mohammad, Galehdari, Hamid, Sedaghat, Alireza, Abdorasuli, Nehzat
Format: Artigo
Sprache:Inglês
Veröffentlicht: John Wiley and Sons Inc. 2018
Schlagworte:
Case Reports
Online Zugang: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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