Literature DB >> 11950868

Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects.

R Voigt, M Maier-Weidmann, P E Lange, T Haaf.   

Abstract

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Year:  2002        PMID： 11950868      PMCID： PMC1735086          DOI： 10.1136/jmg.39.4.e16

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  2 in total

1.  Chromosomal abnormalities among children born with conotruncal cardiac defects.

Authors:  Edward J Lammer; Jacqueline S Chak; David M Iovannisci; Kathleen Schultz; Kazutoyo Osoegawa; Wei Yang; Suzan L Carmichael; Gary M Shaw
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2009-01

2.  LINE-1 methylation status and its association with tetralogy of fallot in infants.

Authors:  Wei Sheng; Huijun Wang; Xiaojing Ma; Yanyan Qian; Ping Zhang; Yao Wu; Fengyun Zheng; Long Chen; Guoying Huang; Duan Ma
Journal:  BMC Med Genomics       Date:  2012-06-06       Impact factor: 3.063
  2 in total

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