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Copy number analysis of NIPBL in a cohort of 510 patients reveals rare copy number variants and a mosaic deletion.

Published Date 
2014
Categories 
Congenital Malformations
Authors/Supporting Info 
18. Cheng, YW, Tan, CA, Minor, A, Arndt, K, Wysinger, L, Grange, DK, Kozel, BA, Robin, NH, Waggoner, D, Fitzpatrick, C, Das, S, del Gaudio, D. Mol. Genet. Genomic Med. 2014, 2(2):115-23.
Research Link 
http://www.ncbi.nlm.nih.gov/pubmed/?term=24689074
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