Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs
对 1000 例超声异常胎儿进行产前 SNP 芯片检测：致病性、意外性和易感性 CNV
期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/ejhg.2015.193
Srebniak, Malgorzata I; Diderich, Karin Em; Joosten, Marieke; Govaerts, Lutgarde Cp; Knijnenburg, Jeroen; de Vries, Femke At; Boter, Marjan; Lont, Debora; Knapen, Maarten Fcm; de Wit, Merel C; Go, Attie Tji; Galjaard, Robert-Jan H; Van Opstal, Diane
