Aortopathy in the 7q11.23 microduplication syndrome-Reference-Cited by-同舟云学术

Aortopathy in the 7q11.23 microduplication syndrome

Published:2014-11-26 Issue:2 Volume:167 Page:363-370
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Parrott Ashley¹,James Jeanne¹,Goldenberg Paula¹,Hinton Robert B.¹,Miller Erin¹,Shikany Amy¹,Aylsworth Arthur S.²³,Kaiser-Rogers Kathleen²³⁴,Ferns Sunita J.²,Lalani Seema R.⁵,Ware Stephanie M.⁶

Affiliation:

1. Department of Pediatrics; Cincinnati Children's Hospital Medical Center; Heart Institute; Cincinnati Ohio

2. Department of Pediatrics; University of North Carolina; Chapel Hill North Carolina

3. Department of Genetics; University of North Carolina; Chapel Hill North Carolina

4. Department of Pathology and Laboratory Medicine; University of North Carolina; Chapel Hill North Carolina

5. Department of Molecular and Human Genetics; Baylor College of Medicine; Houston Texas

6. Department of Pediatrics and Medical and Molecular Genetics; Indiana University School of Medicine; Indianapolis Indiana

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36859/fullpdf

Reference19 articles.

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2. Detection of clinically relevant exonic copy-number changes by array CGH;Boone;Hum Mutat,2010

3. Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities;Brunetti-Pierri;Nat Genet,2008

4. 7q11.23 Microduplication: a recognizable phenotype;Dixit;Clin Genet,2013

5. Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene;Ewart;J Clin Invest,1994

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3. Intrauterine phenotype features of fetuses with 7q11.23 microduplication syndrome;Orphanet Journal of Rare Diseases;2023-09-27

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