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 *

97 related articles for article (PubMed ID: 1944474)

  • 21. Population screening for fragile-X syndrome.
    Bonthron D; Strain L
    Lancet; 1993 Mar; 341(8847):769-70. PubMed ID: 8095681
    [No Abstract]   [Full Text] [Related]  

  • 22. [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]  

  • 23. Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis.
    Vincent A; Heitz D; Petit C; Kretz C; Oberlé I; Mandel JL
    Nature; 1991 Feb; 349(6310):624-6. PubMed ID: 1672039
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. [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]  

  • 26. Evidence of founder chromosomes in fragile X syndrome.
    Richards RI; Holman K; Friend K; Kremer E; Hillen D; Staples A; Brown WT; Goonewardena P; Tarleton J; Schwartz C
    Nat Genet; 1992 Jul; 1(4):257-60. PubMed ID: 1302021
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Diagnostic tests for fragile X syndrome.
    Oostra BA; Willemsen R
    Expert Rev Mol Diagn; 2001 Jul; 1(2):226-32. PubMed ID: 11901818
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal carrier testing for fragile X: counseling issues and challenges.
    Musci TJ; Moyer K
    Obstet Gynecol Clin North Am; 2010 Mar; 37(1):61-70, Table of Contents. PubMed ID: 20494258
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prenatal diagnosis of a hypermethylated full fragile X mutation in chorionic villi of a male fetus.
    Suzumori K; Yamauchi M; Seki N; Kondo I; Hori T
    J Med Genet; 1993 Sep; 30(9):785-7. PubMed ID: 8411077
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [X fragile syndrome; how to make a precocious diagnostic].
    Gérard-Blanluet M
    Rev Prat; 2005 Jan; 55(1):7-12. PubMed ID: 15801390
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. [Last advances in Fragile X chromosome syndrome].
    Bañares VG
    Medicina (B Aires); 1995; 55(5 Pt 1):457-66. PubMed ID: 8728777
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [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]  

  • 35. From hemophilia B to hemophilia A via the fragile X locus: genes and recombination in the distal region of the human X chromosome long arm.
    Oberlé I; Mandel JL
    Horiz Biochem Biophys; 1986; 8():51-89. PubMed ID: 2875934
    [No Abstract]   [Full Text] [Related]  

  • 36. Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG.
    Sermon K; Seneca S; Vanderfaeillie A; Lissens W; Joris H; Vandervorst M; Van Steirteghem A; Liebaers I
    Prenat Diagn; 1999 Dec; 19(13):1223-30. PubMed ID: 10660959
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Molecular pathology of the fragile X syndrome.
    Tsongalis GJ; Silverman LM
    Arch Pathol Lab Med; 1993 Nov; 117(11):1121-5. PubMed ID: 8239933
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Unstable DNA sequence and methylation in fragile X syndrome].
    Fu SD; Shen Y; Fan Y
    Zhonghua Yi Xue Za Zhi; 1994 Oct; 74(10):611-4, 646-7. PubMed ID: 7842338
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [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]  

    [Previous]   [Next]    [New Search]
    of 5.