Copy Number Variants in Short Children Born Small for Gestational Age

BACKGROUND/AIMS: In addition to Genome-Wide Association studies (GWAS) height-associated genes may be uncovered by studying individuals with extreme short or tall stature. METHODS: Genome-wide analysis for copy number variants (CNVs), using Single Nucleotide Polymorphism (SNP) arrays, was performed...

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Bibliographic Details
Published in:	Horm Res Paediatr
Main Authors:	Wit, Jan M., van Duyvenvoorde, Hermine A., van Klinken, Jan B., Caliebe, Janina, Bosch, Cathy A.J., Lui, Julian C., Gijsbers, Antoinet C.J., Bakker, Egbert, Breuning, Martijn H., Oostdijk, Wilma, Losekoot, Monique, Baron, Jeffrey, Binder, Gerhard, Ranke, Michael B., Ruivenkamp, Claudia A.L.
Format:	Artigo
Language:	Inglês
Published:	2014
Subjects:	Article
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC4236248/ https://ncbi.nlm.nih.gov/pubmed/25300501 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000367712
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Copy Number Variants in Short Children Born Small for Gestational Age

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