A Common Molecular Mechanism Underlies Two Phenotypically Distinct 17p13.1 Microdeletion Syndromes


Adam Shlien,Berivan Baskin,Maria Isabel W. Achatz,Dimitrios J. Stavropoulos,Kim E. Nichols,Louanne Hudgins,Chantal F. Morel,Margaret P. Adam,Nataliya Zhukova,Lianne Rotin,Ana Novokmet,Harriet Druker,Mary Shago,Peter N. Ray,Pierre Hainaut,David Malkin


The American Journal of Human Genetics




12 November 2010

Copyright © 2010, Elsevier

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