Prenatally diagnosed submicroscopic familial aberrations at 18p11.32 without phenotypic effect
产前诊断发现18p11.32位点存在亚显微家族性异常，但无表型效应。
期刊:Molecular Cytogenetics
影响因子:1.4
doi:10.1186/1755-8166-4-27
Srebniak, Malgorzata I; Boter, Marjan; Verboven-Peerden, Carla Ma; Looye-Bruinsma, Gerda Ag; Oudesluijs, Gretel; Galjaard, Robert-Jan H; Van Opstal, Diane
