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11. Clinical utility of array comparative genomic hybridisation in prenatal setting. Lovrecic L; Remec ZI; Volk M; Rudolf G; Writzl K; Peterlin B BMC Med Genet; 2016 Nov; 17(1):81. PubMed ID: 27846804 [TBL] [Abstract][Full Text] [Related]
12. The epidemic of abnormal copy number variant cases missed because of reliance upon noninvasive prenatal screening. Evans MI; Andriole S; Curtis J; Evans SM; Kessler AA; Rubenstein AF Prenat Diagn; 2018 Sep; 38(10):730-734. PubMed ID: 30187534 [TBL] [Abstract][Full Text] [Related]
13. Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases. Fiorentino F; Caiazzo F; Napolitano S; Spizzichino L; Bono S; Sessa M; Nuccitelli A; Biricik A; Gordon A; Rizzo G; Baldi M Prenat Diagn; 2011 Dec; 31(13):1270-82. PubMed ID: 22034057 [TBL] [Abstract][Full Text] [Related]
14. Prenatal microarray comparative genomic hybridization: Experience from the two first years of activity at the Lyon university-hospital. Pons L; Till M; Alix E; Abel C; Boggio D; Bordes A; Caloone J; Raskin FC; Chatron N; Cordier MP; Fichez A; Labalme A; Lajeunesse C; Liaras É; Massoud M; Miribel J; Ollagnon E; Schluth-Bolard C; Vichier-Cerf A; Edery P; Attia J; Huissoud C; Rudigoz RC; Massardier J; Gaucherand P; Sanlaville D J Gynecol Obstet Hum Reprod; 2017 Mar; 46(3):275-283. PubMed ID: 28403926 [TBL] [Abstract][Full Text] [Related]
15. Prenatal and postnatal findings in small-for-gestational-age fetuses without structural ultrasound anomalies at 18-24 weeks. de Wit MC; Srebniak MI; Joosten M; Govaerts LC; Kornelisse RF; Papatsonis DN; de Graaff K; Knapen MF; Bruggenwirth HT; de Vries FA; Van Veen S; Van Opstal D; Galjaard RJ; Go AT Ultrasound Obstet Gynecol; 2017 Mar; 49(3):342-348. PubMed ID: 27102944 [TBL] [Abstract][Full Text] [Related]
16. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency. Chen CP; Lin CJ; Chen YN; Chern SR; Chen SW; Lai ST; Wu PS; Chen LF; Wang W Taiwan J Obstet Gynecol; 2017 Jun; 56(3):398-401. PubMed ID: 28600059 [TBL] [Abstract][Full Text] [Related]
17. The Integration of Noninvasive Prenatal Screening into the Existing Prenatal Paradigm: a Survey of Current Genetic Counseling Practice. Suskin E; Hercher L; Aaron KE; Bajaj K J Genet Couns; 2016 Oct; 25(5):1032-43. PubMed ID: 26879922 [TBL] [Abstract][Full Text] [Related]
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20. [Application of array comparative genomic hybridization analysis for fetuses with growth anomalies]. Wang L; Wang X; Cai N; He B; Wu Q; Li W; Zhang L; Ma X; Qiang R Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):691-694. PubMed ID: 28981935 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]