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.

Detalles Bibliográficos
Autores principales: Shariati, Gholamreza, Saberi, Alihossein, Hamid, Mohammad, Galehdari, Hamid, Sedaghat, Alireza, Abdorasuli, Nehzat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099003/
https://www.ncbi.nlm.nih.gov/pubmed/30147883
http://dx.doi.org/10.1002/ccr3.1604

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099003/
https://www.ncbi.nlm.nih.gov/pubmed/30147883
http://dx.doi.org/10.1002/ccr3.1604

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