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Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformations
scientific article published on 13 March 2017
Author/s
author: Xia Wang, Lihadh Al-Gazali, James R. Lupski, Richard Gibbs, Donna Muzny, Christine M. Eng, Yaping Yang, Jill A Rosenfeld, Sharon E Plon
Work details
Publication date
March 13, 2017
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Language
English
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