Inv dup(22), del(22)(q11) and r(22) in the father of a child with DiGeorge syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/5200525.pdf
Cited by 11 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. Oculo-auriculo-vertebral spectrum, cat eye, and distal 22q11 microdeletion syndromes: A unique double rearrangement;American Journal of Medical Genetics Part A;2013-07-24
2. An unusual chromosome 22q11 deletion associated with an apparent complementary ring chromosome in a phenotypically normal woman;European Journal of Medical Genetics;2011-05
3. 22q11 Deletion Syndrome: A Role for Tbx1 in Pharynx and Cardiovascular Development;eLS;2010-09-15
4. 22q11 Deletion Syndrome: A Role for TBX1 in Pharyngeal and Cardiovascular Development;Pediatric Cardiology;2010-01-07
5. Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversion;European Journal of Human Genetics;2008-10-15
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