Microdeletion 22q11 in complex cardiovascular malformations-Reference-Cited by-同舟云学术

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Microdeletion 22q11 in complex cardiovascular malformations

Published:1997-03-17 Issue:4 Volume:99 Page:433-442
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Mehraein Yasmin,Wippermann C.-F.,Michel-Behnke Ina,Ngo Thi Kim Nhan,Hillig Ulrike,Giersberg Marina,Aulepp Ute,Barth H.,Fritz Barbara,Rehder H.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390050385.pdf

Cited by 55 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. Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review;American Journal of Medical Genetics Part A;2017-11-21

2. Syndromic Congenital Heart Diseases;Comprehensive Approach to Adult Congenital Heart Disease;2014

3. Can clinical assessment detect 22q11.2 deletions in patients with cardiac malformations? A review;European Journal of Medical Genetics;2011-01

4. Síndrome de deleção 22q11 e cardiopatias congênitas complexas;Revista da Associação Médica Brasileira;2011-01

5. 22q11.2 deletion syndrome and complex congenital heart defects;Revista da Associação Médica Brasileira (English Edition);2011-01

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