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5. [Fetal blood sampling for karyotype using echoguided puncture of the cord. Study of 103 pregnancies]. Boulot P; Courtieu C; Lefort G; Deschamps F; Sarda P; Galand B; Mares P; Hedon B; Laffargue F; Viala JL J Gynecol Obstet Biol Reprod (Paris); 1989; 18(8):1007-15. PubMed ID: 2695568 [TBL] [Abstract][Full Text] [Related]
6. Intrauterine diagnosis of chromosome anomalies. Karjalainen O; Aula P Ann Chir Gynaecol Fenn; 1975; 64(3):146-51. PubMed ID: 130086 [TBL] [Abstract][Full Text] [Related]
7. Management of prenatally detected nonlethal fetal anomalies: is a karyotype of benefit? Brumfield CG; Davis RO; Hauth JC; Cosper P; Colvin EV; Finley SC Am J Perinatol; 1991 Jul; 8(4):255-8. PubMed ID: 1741869 [TBL] [Abstract][Full Text] [Related]
8. Abnormal pregnancy sonogram and chromosomal anomalies: four years' experience with rapid karyotyping. Hentemann M; Rauskolb R; Ulbrich R; Bartels I Prenat Diagn; 1989 Sep; 9(9):605-12. PubMed ID: 2678086 [TBL] [Abstract][Full Text] [Related]
9. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations]. Ulmer R; Pfeiffer RA; Kollert A; Beinder E Z Geburtshilfe Neonatol; 2000; 204(1):1-7. PubMed ID: 10721179 [TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis by chorionic villus sampling: lessons of the first 600 cases. Hogge WA; Schonberg SA; Golbus MS Prenat Diagn; 1985; 5(6):393-400. PubMed ID: 4088973 [TBL] [Abstract][Full Text] [Related]
12. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing. Wang J; Chen L; Zhou C; Wang L; Xie H; Xiao Y; Zhu H; Hu T; Zhang Z; Zhu Q; Liu Z; Liu S; Wang H; Xu M; Ren Z; Yu F; Cram DS; Liu H Am J Obstet Gynecol; 2018 Sep; 219(3):287.e1-287.e18. PubMed ID: 29852155 [TBL] [Abstract][Full Text] [Related]
13. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester]. Zhang YP; Wu JP; Li XT; Lei CX; Xu JZ; Yin M Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986 [TBL] [Abstract][Full Text] [Related]
14. Prenatal cytogenetic abnormalities: correlations of structural rearrangements and ultrasonographically detected fetal anomalies. Hume RF; Kilmer-Ernst P; Wolfe HM; Ebrahim SA; Treadwell MC; Johnson MP; Evans MI Am J Obstet Gynecol; 1995 Oct; 173(4):1334-6. PubMed ID: 7485349 [TBL] [Abstract][Full Text] [Related]
15. Prospective ranking of the sonographic markers for aneuploidy: data of 2143 prenatal cytogenetic diagnoses referred for abnormalities on ultrasound. Daniel A; Athayde N; Ogle R; George AM; Michael J; Pertile MD; Bryan J; Jammu V; Trudinger BJ Aust N Z J Obstet Gynaecol; 2003 Feb; 43(1):16-26. PubMed ID: 12755342 [TBL] [Abstract][Full Text] [Related]
16. Rapid karyotyping in fetuses with abnormal sonogram. Hsieh FJ; Hsu HC; Ko TM; Chang FM; Chen HY; Jean HH; Chuang SM Acta Obstet Gynecol Scand; 1988; 67(7):621-5. PubMed ID: 3073624 [TBL] [Abstract][Full Text] [Related]
17. Fetal malformations and abnormalities. Laurence KM Lancet; 1974 Oct; 2(7886):939-42. PubMed ID: 4138563 [No Abstract] [Full Text] [Related]
18. Results and pitfalls in prenatal cytogenetic diagnosis. Hsu LY; Dubin EC; Kerenyi T; Hirschhorn K J Med Genet; 1973 Jun; 10(2):112-9. PubMed ID: 4268389 [TBL] [Abstract][Full Text] [Related]
19. Risk for chromosome abnormality at amniocentesis following a child with a non-inherited chromosome aberration. A European Collaborative Study on Prenatal Diagnoses 1981. Stene J; Stene E; Mikkelsen M Prenat Diagn; 1984; 4 Spec No():81-95. PubMed ID: 6235486 [TBL] [Abstract][Full Text] [Related]
20. Parental decision following prenatal diagnosis of fetal chromosome abnormality. Verp MS; Bombard AT; Simpson JL; Elias S Am J Med Genet; 1988 Mar; 29(3):613-22. PubMed ID: 3377004 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]