BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 3456685)

  • 1. [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]  

  • 2. [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]  

  • 3. [The role of the marker X chromosome in the diagnosis of Martin-Bell syndrome (review of the literature)].
    Bessudnova SS; Il'inskikh NN
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1990; 90(3):128-32. PubMed ID: 2163154
    [No Abstract]   [Full Text] [Related]  

  • 4. Prenatal diagnosis of fragile (X) syndrome.
    Hogge WA; Schonberg SA; Glover TW; Hecht F; Golbus MS
    Obstet Gynecol; 1984 Mar; 63(3 Suppl):19S-21S. PubMed ID: 6700875
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The fragile X chromosome.
    N Engl J Med; 1987 Feb; 316(8):483. PubMed ID: 3807989
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. [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]  

  • 8. 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]  

  • 9. Experience with prenatal fragile X detection.
    Jenkins EC; Brown WT; Brooks J; Duncan CJ; Rudelli RD; Wisniewski HM
    Am J Med Genet; 1984 Jan; 17(1):215-39. PubMed ID: 6711597
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fragile X syndrome.
    de la Cruz FF
    Am J Ment Defic; 1985 Sep; 90(2):119-23. PubMed ID: 3901755
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular diagnosis of the fragile X [Fra (X)] syndrome: calculation of risks based on flanking DNA markers in small phase-unknown families.
    Bridge PJ; Lillicrap DP
    Am J Med Genet; 1989 May; 33(1):92-9. PubMed ID: 2568753
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of the fragile X syndrome using fetal blood and amniotic fluid.
    Webb TP; Rodeck CH; Nicolaides KH; Gosden CM
    Prenat Diagn; 1987 Mar; 7(3):203-14. PubMed ID: 3588539
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Mental retardation and the fragile X syndrome].
    Veenema H; Geraedts JP
    Ned Tijdschr Geneeskd; 1984 Mar; 128(13):618-21. PubMed ID: 6717630
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. Prenatal diagnosis of the fragile-X in male monozygotic twins: discordant expression of the fragile site in amniocytes.
    Rocchi M; Pecile V; Archidiacono N; Monni G; Dumez Y; Filippi G
    Prenat Diagn; 1985; 5(3):229-31. PubMed ID: 4022944
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The fragile X syndrome I: familial variation in the proportion of lymphocytes with the fragile site in males.
    Soudek D; Partington MW; Lawson JS
    Am J Med Genet; 1984 Jan; 17(1):241-52. PubMed ID: 6711598
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [The adult mentally handicapped in psychiatry. Etiologic study with research on the fragile X chromosome].
    Ferauge M
    Acta Psychiatr Belg; 1986; 86(3):287-96. PubMed ID: 3751650
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Fragile-X syndrome: an overview.
    Brady MA
    Pediatr Nurs; 1984; 10(3):210-1. PubMed ID: 6563510
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.