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A small terminal deletion 11q in a boy without Jacobsen syndrome: narrowing the critical region for the 11q Jacobsen syndrome phenotype.

作者信息

Evers Christina, Janssen Johannes W G, Jauch Anna, Bonin Michael, Moog Ute

机构信息

Institute of Human Genetics, Heidelberg University, Heidelberg, Germany.

出版信息

Am J Med Genet A. 2012 Mar;158A(3):680-4. doi: 10.1002/ajmg.a.34433. Epub 2012 Feb 2.

DOI:10.1002/ajmg.a.34433
PMID:22302716
Abstract
摘要

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引用本文的文献

[1]
Trisomy 1q32 and monosomy 11q25 associated with congenital heart defect: cytogenomic delineation and patient fourteen years follow-up.

Mol Cytogenet. 2014-8-22

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