A common molecular mechanism underlies two phenotypically distinct 17p13.1 microdeletion syndromes
两种表型不同的17p13.1微缺失综合征具有共同的分子机制。
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2010.10.007
Shlien, Adam; Baskin, Berivan; Achatz, Maria Isabel W; Stavropoulos, Dimitrios J; Nichols, Kim E; Hudgins, Louanne; Morel, Chantal F; Adam, Margaret P; Zhukova, Nataliya; Rotin, Lianne; Novokmet, Ana; Druker, Harriet; Shago, Mary; Ray, Peter N; Hainaut, Pierre; Malkin, David