Subtelomeric deletions of chromosome 6p: Molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher?Schinzel (3C) syndrome-Reference-Cited by-同舟云学术

Subtelomeric deletions of chromosome 6p: Molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher?Schinzel (3C) syndrome

Published:2005 Issue:1 Volume:134A Page:3-11
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

DeScipio Cheryl,Schneider Lori,Young Terri L.,Wasserman Nora,Yaeger Dinah,Lu Fengmin,Wheeler Patricia G.,Williams Marc S.,Bason Lynn,Jukofsky Lori,Menon Ammini,Geschwindt Ryan,Chudley Albert E.,Saraiva Jorge,Schinzel Albert A. G. L.,Guichet Agnes,Dobyns William E.,Toutain Annick,Spinner Nancy B.,Krantz Ian D.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference17 articles.

1. Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment

2. Molecular characterization of partial trisomy 16q24.1-qter: Clinical report and review of the literature

3. Delineation of two distinct 6p deletion syndromes

4. Telomeres: a diagnosis at the end of the chromosomes

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