Molecular characterisation of a prenatally diagnosed 5q15q21.3 deletion and review of the literature-Reference-Cited by-同舟云学术

Molecular characterisation of a prenatally diagnosed 5q15q21.3 deletion and review of the literature

Published:2006 Issue:3 Volume:26 Page:231-238
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Malan Valérie,Martinovic Jelena,Sanlaville Damien,Caillat Stéphanie,Perrier Waill Marie-Christine,Maurin Ganne Marie-Laure,Tantau Julia,Attie-Bitach Tania,Vekemans Michel,Morichon-Delvallez Nicole

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference38 articles.

1. Adenomatous polyposis coli and a cytogenetic deletion of chromosome 5 resulting from a maternal intrachromosomal insertion.

2. Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly

3. An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations.

4. Double chromosome anomaly: Interstitial deletion 5q and reciprocal translocation (1;11) (p22;q21)

5. Interstitial deletion of band q12 of chromosome 5

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