Molecular genetics of 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

Molecular genetics of 22q11.2 deletion syndrome

Published:2018-10 Issue:10 Volume:176 Page:2070-2081
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Morrow Bernice E.¹^ORCID,McDonald-McGinn Donna M.²,Emanuel Beverly S.²,Vermeesch Joris R.³,Scambler Peter J.⁴

Affiliation:

1. Department of Genetics; Albert Einstein College of Medicine; Bronx New York

2. Division of Human Genetics, Children's Hospital of Philadelphia and Department of Pediatrics, Perelman School of Medicine; University of Pennsylvania; Philadelphia

3. Center for Human Genetics; Katholieke Universiteit Leuven (KU Leuven); Leuven Belgium

4. Institute of Child Health; University College London; London UK

Funder

British Heart Foundation

Fondation Jérôme Lejeune

Fondation Leducq

National Heart, Lung, and Blood Institute

National Institute of Child Health and Human Development

National Institute of Mental Health

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.40504/fullpdf

Reference144 articles.

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3. Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations;Arnold;Development,2006

4. Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution;Babcock;Genome Research,2003

5. Hominoid lineage specific amplification of low-copy repeats on 22q11.2 (LCR22s) associated with velo-cardio-facial/digeorge syndrome;Babcock;Human Molecular Genetics,2007

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