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2. Experience with multiple approaches to the prenatal diagnosis of the fragile X syndrome: amniotic fluid, chorionic villi, fetal blood and molecular methods. Shapiro LR; Wilmot PL; Murphy PD; Breg WR Am J Med Genet; 1988; 30(1-2):347-54. PubMed ID: 2902794 [TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of fragile X syndrome by placental (chorionic villi) biopsy culture. McKinley MJ; Kearney LU; Nicolaides KH; Gosden CM; Webb TP; Fryns JP Am J Med Genet; 1988; 30(1-2):355-68. PubMed ID: 3177458 [TBL] [Abstract][Full Text] [Related]
4. Polymorphic DNA markers in prenatal diagnosis of fragile X syndrome. Oberlé I; Mandel JL; Boué J; Mattei MG; Mattei JF Lancet; 1985 Apr; 1(8433):871. PubMed ID: 2858726 [No Abstract] [Full Text] [Related]
5. First trimester prenatal diagnosis of a male fetus with fragile X. Tommerup N; Søndergaard F; Tønnesen T; Kristensen M; Arveiler B; Schinzel A Lancet; 1985 Apr; 1(8433):870. PubMed ID: 2858725 [No Abstract] [Full Text] [Related]
6. Prenatal diagnosis of fragile X in a heterozygous female fetus and postnatal follow-up. Wilson MG; Marchese CA Prenat Diagn; 1984; 4(1):61-6. PubMed ID: 6728827 [TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of the fragile X using thymidine induction. Sutherland GR; Baker E; Purvis-Smith S; Hockey A; Krumins E; Eichenbaum SZ Prenat Diagn; 1987 Mar; 7(3):197-202. PubMed ID: 2954037 [TBL] [Abstract][Full Text] [Related]
8. [Prenatal diagnosis in a family carrying the fragile X syndrome using recombinant DNA technics]. Benítez J; Fernández E; Ramos C; Nunes V; del Río E; Baiget M Rev Clin Esp; 1989 Apr; 184(7):364-6. PubMed ID: 2570446 [TBL] [Abstract][Full Text] [Related]
9. Recent experience in prenatal fra(X) detection. Jenkins EC; Brown WT; Krawczun MS; Duncan CJ; Lele KP; Cantu ES; Schonberg S; Golbus MS; Sekhon GS; Stark S Am J Med Genet; 1988; 30(1-2):329-36. PubMed ID: 2972205 [TBL] [Abstract][Full Text] [Related]
10. [Fetal chromosome abnormalities diagnosed by chorionic villi sampling]. Gardó S; Bajnóczky K; Nagy M; Nagy S Orv Hetil; 1993 Oct; 134(44):2427-30. PubMed ID: 8233461 [TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of the fragile X--the Australasian experience. Purvis-Smith SG; Laing S; Sutherland GR; Baker E Am J Med Genet; 1988; 30(1-2):337-45. PubMed ID: 3177457 [TBL] [Abstract][Full Text] [Related]
12. A confirmed prenatal diagnosis of a female fetus with the fragile X chromosome. Venter PA; Coetzee DJ; Badenhorst A; Marx MP; Op't Hof J; Behari D; Wilmot J; Battson SA Prenat Diagn; 1984; 4(6):473-4. PubMed ID: 6522350 [No Abstract] [Full Text] [Related]
13. 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]
16. Prenatal diagnosis of X-linked mental retardation with fragile (X) using fetoscopy and fetal blood sampling. Webb T; Gosden CM; Rodeck CH; Hamill MA; Eason PE Prenat Diagn; 1983; 3(2):131-7. PubMed ID: 6622392 [TBL] [Abstract][Full Text] [Related]
17. The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosis. Butler MG; Dev VG; Shah D; Ulm JE; Wilmot PL; Shapiro LR Am J Med Genet; 1988 Dec; 31(4):775-8. PubMed ID: 3239566 [TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of fragile X syndrome: management of the male fetus with a premutation. Strain L; Porteous ME; Gosden CM; Ellis PM; Neilson JP; Bonthron DT Prenat Diagn; 1994 Jun; 14(6):469-74. PubMed ID: 7937584 [TBL] [Abstract][Full Text] [Related]
19. [Prenatal diagnosis of fragile X syndrome--Martin-Bell syndrome]. Lindenberg S; Andersen AM; Thomsen SG; van der Hagen CB Ugeskr Laeger; 1986 Jan; 148(3):134-5. PubMed ID: 3456685 [No Abstract] [Full Text] [Related]
20. Fragile X syndrome. McKinley MJ; Nicolaides KH; Kearney LU; Heron O Br Med J (Clin Res Ed); 1987 Oct; 295(6603):922. PubMed ID: 3119101 [No Abstract] [Full Text] [Related] [Next] [New Search]