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8. The prenatal detection of the fragile X chromosome: review of recent experience. Jenkins EC; Brown WT; Wilson MG; Lin MS; Alfi OS; Wassman ER; Brooks J; Duncan CJ; Masia A; Krawczun MS Am J Med Genet; 1986; 23(1-2):297-311. PubMed ID: 2937295 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. The fragile X chromosome. N Engl J Med; 1987 Feb; 316(8):483. PubMed ID: 3807989 [No Abstract] [Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. Prenatal diagnosis of the fra(X) syndrome. Shapiro LR; Wilmot PL Am J Med Genet; 1986; 23(1-2):325-40. PubMed ID: 3953652 [TBL] [Abstract][Full Text] [Related]
15. Second trimester prenatal diagnosis of the fragile X. Tommerup N; Aula P; Gustavii B; Heiberg A; Holmgren G; von Koskull H; Leisti J; Mikkelsen M; Mitelman F; Nielsen KB Am J Med Genet; 1986; 23(1-2):313-24. PubMed ID: 2937296 [TBL] [Abstract][Full Text] [Related]
16. [Successful prenatal diagnosis of the fragile X chromosome without the use of folic acid antagonists]. Macek M; Nedomová V; Bavorová H; Loucková M; Chudoba D; Seemanová E; Schmidtová A; Passarge E Cesk Pediatr; 1983 Sep; 38(9):525-7. PubMed ID: 6640753 [No Abstract] [Full Text] [Related]
17. An important clinical approach in detecting the fragile X syndrome. Milunsky A Am J Public Health; 1985 Jul; 75(7):715-6. PubMed ID: 4003647 [No Abstract] [Full Text] [Related]
18. Fragile X syndrome. Halstead S J R Soc Med; 1990 Jun; 83(6):415. PubMed ID: 2380976 [No Abstract] [Full Text] [Related]
19. [Prenatal diagnosis of a male fetal carrier of fragile X chromosome by the amniotic fluid cells]. Tejada I; Boué J; Gilgenkrantz S Ann Genet; 1983; 26(4):247-50. PubMed ID: 6607707 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]