Unusual dicentric chromosome 22 associated with a 22q13 deletion-Reference-Cited by-同舟云学术

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Unusual dicentric chromosome 22 associated with a 22q13 deletion

Published:2006 Issue:24 Volume:140A Page:2819-2823
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Babineau Tina,Wilson Heather L.,Dawson Angelika J.,Chodirker Bernard N.,Der Kaloustian Vazken M.,Demczuk Suzanne,McDermid Heather E.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference22 articles.

1. Disruption of the ProSAP2 Gene in a t(12;22)(q24.1;q13.3) Is Associated with the 22q13.3 Deletion Syndrome

2. Cryptic terminal rearrangement of chromosome 22q13.32 detected by FISH in two unrelated patients.

3. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

4. Analysis of the Cat Eye Syndrome Critical Region in Humans and the Region of Conserved Synteny in Mice: A Search for Candidate Genes at or near the Human Chromosome 22 Pericentromere

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. DELETION 22q13 SYNDROME;Cassidy and Allanson's Management of Genetic Syndromes;2020-10-30

2. Deletion 22q13 Syndrome: Phelan-McDermid Syndrome;Management of Genetic Syndromes;2010-05-17

3. A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter→22q12.1: Clinical, cytogenetic and molecular observations;European Journal of Medical Genetics;2008-07

4. Recombination of a maternal pericentric inversion results in 22q13 deletion syndrome;Clinical Dysmorphology;2008-01

5. 22q13.3 deletion syndrome: A recognizable malformation syndrome associated with marked speech and language delay;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2007

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