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Left ventricular noncompaction: A rare disorder in adults and its association with 1p36 chromosomal anomaly

  • Published:2009-12-23 Issue:1 Volume:152A Page:191-195
  • ISSN:1552-4825
  • Container-title:American Journal of Medical Genetics Part A
  • language:en
  • Short-container-title:Am. J. Med. Genet.

Author:

Dod Harvinder S.,Bhardwaj Ravindra,Hummel Marybeth,Morise Anthony P.,Batish Satdev,Warden Bradford E.,Beto Robert J.,Jain Abnash C.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 5 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. Cardiovascular Phenotypic Spectrum of 1p36 Deletion Syndrome;Journal of Pediatric Genetics;2021-07-29

2. Delineating the phenotype of 1p36 deletion in adolescents and adults;American Journal of Medical Genetics Part A;2014-07-08

3. Genetics of cardiomyopathies in children;Cardiogenetics;2011-08-17

4. Epidemiology of Ebstein anomaly: Prevalence and patterns in Texas, 1999-2005;American Journal of Medical Genetics Part A;2011-04-04

5. Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints;American Journal of Medical Genetics Part A;2010-11-24
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