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, HarriVolume:
87
Year:
2010
Language:
english
Pages:
12
DOI:
10.1016/j.ajhg.2010.10.007
File:
PDF, 860 KB
english, 2010