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
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author Shariati, Gholamreza
Saberi, Alihossein
Hamid, Mohammad
Galehdari, Hamid
Sedaghat, Alireza
Abdorasuli, Nehzat
author_facet Shariati, Gholamreza
Saberi, Alihossein
Hamid, Mohammad
Galehdari, Hamid
Sedaghat, Alireza
Abdorasuli, Nehzat
author_sort Shariati, Gholamreza
collection PubMed
description 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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spelling pubmed-60990032018-08-24 Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH Shariati, Gholamreza Saberi, Alihossein Hamid, Mohammad Galehdari, Hamid Sedaghat, Alireza Abdorasuli, Nehzat Clin Case Rep Case Reports 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. John Wiley and Sons Inc. 2018-06-13 /pmc/articles/PMC6099003/ /pubmed/30147883 http://dx.doi.org/10.1002/ccr3.1604 Text en © 2018 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Reports
Shariati, Gholamreza
Saberi, Alihossein
Hamid, Mohammad
Galehdari, Hamid
Sedaghat, Alireza
Abdorasuli, Nehzat
Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH
title Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH
title_full Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH
title_fullStr Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH
title_full_unstemmed Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH
title_short Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH
title_sort prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array cgh
topic Case Reports
url 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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