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4. Nuchal translucency and other first-trimester sonographic markers of chromosomal abnormalities. Nicolaides KH Am J Obstet Gynecol; 2004 Jul; 191(1):45-67. PubMed ID: 15295343 [TBL] [Abstract][Full Text] [Related]
5. Integrated ultrasound and biochemical screening for trisomy 21 using fetal nuchal translucency, absent fetal nasal bone, free beta-hCG and PAPP-A at 11 to 14 weeks. Cicero S; Bindra R; Rembouskos G; Spencer K; Nicolaides KH Prenat Diagn; 2003 Apr; 23(4):306-10. PubMed ID: 12673635 [TBL] [Abstract][Full Text] [Related]
6. A screening program for trisomy 21 at 10-14 weeks using fetal nuchal translucency, maternal serum free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A. Spencer K; Souter V; Tul N; Snijders R; Nicolaides KH Ultrasound Obstet Gynecol; 1999 Apr; 13(4):231-7. PubMed ID: 10341399 [TBL] [Abstract][Full Text] [Related]
7. First-trimester nuchal translucency and maternal serum biochemical screening for Down's syndrome: a happy union? Thilaganathan B Ultrasound Obstet Gynecol; 1999 Apr; 13(4):229-30. PubMed ID: 10341398 [No Abstract] [Full Text] [Related]
8. [Trisomy 21 screening: value of ultrasound and serum markers in a combined approach]. Senat MV; Rozenberg P; Bernard JP; Ville Y J Gynecol Obstet Biol Reprod (Paris); 2001 Feb; 30(1):11-27. PubMed ID: 11240502 [No Abstract] [Full Text] [Related]
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10. Nasal bone in first-trimester screening for trisomy 21. Cicero S; Avgidou K; Rembouskos G; Kagan KO; Nicolaides KH Am J Obstet Gynecol; 2006 Jul; 195(1):109-14. PubMed ID: 16813749 [TBL] [Abstract][Full Text] [Related]
11. Uptake of prenatal screening for chromosomal anomalies: impact of test results in a previous pregnancy. Spencer K Prenat Diagn; 2002 Dec; 22(13):1229-32. PubMed ID: 12478639 [TBL] [Abstract][Full Text] [Related]
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13. The use of nuchal translucency in contemporary obstetric practice. Said S; Malone FD Clin Obstet Gynecol; 2008 Mar; 51(1):37-47. PubMed ID: 18303498 [TBL] [Abstract][Full Text] [Related]
15. One-stop clinic for assessment of risk of chromosomal defects at 12 weeks of gestation. Nicolaides KH; Bindra R; Heath V; Cicero S J Matern Fetal Neonatal Med; 2002 Jul; 12(1):9-18. PubMed ID: 12422904 [TBL] [Abstract][Full Text] [Related]
16. Trisomy 18 in a fetus with normal NT and abnormal maternal serum biochemistry. De Biasio P; Canini S; Prefumo F; Venturini PL Prenat Diagn; 2002 Jun; 22(6):492-3. PubMed ID: 12116311 [No Abstract] [Full Text] [Related]
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20. Screening for chromosomal abnormalities in the first trimester using ultrasound and maternal serum biochemistry in a one-stop clinic: a review of three years prospective experience. Spencer K; Spencer CE; Power M; Dawson C; Nicolaides KH BJOG; 2003 Mar; 110(3):281-6. PubMed ID: 12628268 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]