Author:
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
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference37 articles.
1. Wladimiroff JW, Cohen-Overbeek TE, Ursem NT et al: Twenty years of experience in advanced ultrasound scanning for fetal anomalies in Rotterdam. Ned Tijdschr Geneeskd 2003; 147: 2106–2110.
2. Caron L, Tihy F, Dallaire L : Frequencies of chromosomal abnormalities at amniocentesis: over 20 years of cytogenetic analyses in one laboratory. Am J Med Genet 1999; 82: 149–154.
3. Park SY, Kim JW, Kim YM et al: Frequencies of fetal chromosomal abnormalities at prenatal diagnosis: 10 years experiences in a single institution. J Korean Med Sci 2001; 16: 290–293.
4. Rickman L, Fiegler H, Carter NP et al: Prenatal diagnosis by array-CGH. Eur J Med Genet 2005; 48: 232–240.
5. Hillman SC, Pretlove S, Coomarasamy A et al: Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis. Ultrasound Obstet Gynecol 2011; 37: 6–14.
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