De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency-Reference-Cited by-同舟云学术

De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency

Published:2006 Issue:3 Volume:26 Page:206-213
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Brisset Sophie,Kasakyan Serdar,L'Herminé Aurore Coulomb,Mairovitz Valérie,Gautier Evelyne,Aubry Marie-Cécile,Benkhalifa Moncef,Tachdjian Gérard

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference24 articles.

1. Clinical characteristics associated with dup17(q24q25.1) in a mosaic mother and two nonmosaic daughters

2. Familial cryptic translocation (2;17) ascertained through recurrent spontaneous abortions

3. Duplication of distal 17q from a maternal translocation: an additional case with some unique features.

4. Chromosome Breakage Hotspots and Delineation of the Critical Region for the 9p-Deletion Syndrome

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