These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

75 related articles for article (PubMed ID: 1681307)

  • 21. [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]  

  • 22. Prenatal genetic counseling: what is fragile X?
    Bodurtha J; Tams L; Jackson-Cook C
    Va Med Q; 1992; 119(2):97-8. PubMed ID: 1562624
    [No Abstract]   [Full Text] [Related]  

  • 23. Risk calculation of missed prenatal diagnosis of fragile-X syndrome.
    Oostra BA; Sandkuyl LA; Halley DJ
    Prenat Diagn; 1990 Aug; 10(8):545-6. PubMed ID: 2082996
    [No Abstract]   [Full Text] [Related]  

  • 24. Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection.
    Dobkin C; Ding X; Li S; Houck G; Nolin SL; Glicksman A; Zhong N; Jenkins EC; Brown WT
    Am J Med Genet; 1999 Apr; 83(4):338-41. PubMed ID: 10208176
    [TBL] [Abstract][Full Text] [Related]  

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

  • 26. Economic evaluation of prenatal carrier screening for fragile X syndrome.
    Vintzileos AM; Ananth CV; Fisher AJ; Smulian JC; Day-Salvatore D; Beazoglou T; Knuppel RA
    J Matern Fetal Med; 1999; 8(4):168-72. PubMed ID: 10406300
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [The molecular genetics of the fragile X syndrome. Its molecular diagnosis by DNA probes].
    Giné R; Espinás ML; Antich J; Carballo M
    Med Clin (Barc); 1992 Feb; 98(4):121-4. PubMed ID: 1552760
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Rapid preparation of diagnostic probes for the fragile X syndrome by direct PCR amplification of human chromosomal DNA.
    Yamauchi M; Seki N; Hori T
    Jpn J Hum Genet; 1992 Sep; 37(3):195-203. PubMed ID: 1472701
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis and carrier screening for fragile X by PCR.
    Brown WT; Nolin S; Houck G; Ding X; Glicksman A; Li SY; Stark-Houck S; Brophy P; Duncan C; Dobkin C; Jenkins E
    Am J Med Genet; 1996 Jul; 64(1):191-5. PubMed ID: 8826474
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [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]  

  • 31. Three peaks in the polymerase chain reaction fragile X analysis.
    Sharony R; Shtorch A; Amiel A; Guetta E; Peleg L; Pras E; Ries-Levavi L
    J Med Screen; 2012 Sep; 19(3):112-5. PubMed ID: 23093728
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Problems posed by genetic diseases, concerning DNA instability disorders: fragile X syndrome].
    Lesca G; Rousselle C
    Rev Prat; 2006 Oct; 56(15):1705-10. PubMed ID: 17137259
    [No Abstract]   [Full Text] [Related]  

  • 33. The fragile X syndrome. A peculiar pattern of inheritance.
    Shapiro LR
    N Engl J Med; 1991 Dec; 325(24):1736-8. PubMed ID: 1944474
    [No Abstract]   [Full Text] [Related]  

  • 34. Diagnosing fragile X syndrome.
    Moore DY
    Lancet; 1993 Dec 18-25; 342(8886-8887):1563-4. PubMed ID: 7902945
    [No Abstract]   [Full Text] [Related]  

  • 35. FMRP detection assay for the diagnosis of the fragile X syndrome.
    Willemsen R; Oostra BA
    Am J Med Genet; 2000; 97(3):183-8. PubMed ID: 11449486
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. [Fragile X syndrome: current knowledge].
    Pellissier MC; Voelckel MA; Mattei JF
    Pediatrie; 1992; 47(11):743-50. PubMed ID: 1364151
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Fragile X syndrome and fragile XE mental retardation.
    Sutherland GR; Mulley JC
    Prenat Diagn; 1996 Dec; 16(13):1199-211. PubMed ID: 9061751
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [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]  

  • 40. Fragile X mental retardation syndrome: DNA diagnosis and carrier detection in New Zealand families.
    Neville L; Cochrane J; Fitzgerald P; Kennedy M
    N Z Med J; 1995 Oct; 108(1009):404-6. PubMed ID: 7478333
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.