Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p23.1-Reference-Cited by-同舟云学术

Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p23.1

Published:2011-08-03 Issue:9 Volume:155 Page:2196-2202
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Digilio Maria Cristina,Bernardini Laura,Lepri Francesca,Giuffrida Maria Grazia,Guida Valentina,Baban Anwar,Versacci Paolo,Capolino Rossella,Torres Barbara,De Luca Alessandro,Novelli Antonio,Marino Bruno,Dallapiccola Bruno

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.34131/fullpdf

Reference39 articles.

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2. Del 1p26 syndrome: A newly emerging clinical entity;Battaglia;Brain Dev,2005

3. Further delineation of deletion 1p36 syndrome in 60 patients: A recognizable phenotype and common cause of developmental delay and mental retardation;Battaglia;Pediatrics,2008

4. Syndromic craniosynostosis due to complex chromosome 5 rearrangement and MSX2 gene triplication;Bernardini;Am J Med Genet Part A,2007

5. Noncompaction of the ventricular myocardium is associated with a de novo mutation in the beta-Myosin Heavy Chain Gene;Budde;PloS ONE,2007

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