BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

293 related articles for article (PubMed ID: 3978845)

  • 21. Clinical and cytogenetic survey of institutionalized mentally retarded patients with emphasis on the fragile-X syndrome.
    Butler MG; Singh DN
    J Intellect Disabil Res; 1993 Apr; 37 ( Pt 2)(Pt 2):131-42. PubMed ID: 8481611
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Macroorchidism and fragile X in mentally retarded males. Clinical, cytogenetic, and some hormonal investigations in mentally retarded males, including two with the fragile site at Xq28, fra(X)(q28).
    Nielsen KB; Tommerup N; Dyggve HV; Schou C
    Hum Genet; 1982; 61(2):113-7. PubMed ID: 6215327
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Fragile X chromosome in institutionalized male adults with mental retardation.
    Aoi T; Takashima H; Takada T; Okada T
    Keio J Med; 1989 Mar; 38(1):36-9. PubMed ID: 2785613
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A comparison of language characteristics of mentally retarded adults with fragile X syndrome and those with nonspecific mental retardation and autism.
    Paul R; Dykens E; Leckman JF; Watson M; Breg WR; Cohen DJ
    J Autism Dev Disord; 1987 Dec; 17(4):457-68. PubMed ID: 3479423
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Frequency of the fragile X syndrome in institutionalized mentally retarded females in Japan.
    Arinami T; Kondo I; Nakajima S; Hamaguchi H
    Hum Genet; 1987 Aug; 76(4):344-7. PubMed ID: 3610153
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The inactivation of the fragile X chromosome in female carriers of the Martin Bell syndrome as studied by two different methods.
    Tuckerman E; Webb T
    Clin Genet; 1989 Jul; 36(1):25-30. PubMed ID: 2766560
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The fragile X syndrome in a large family. II. Psychological investigations.
    Veenema H; Veenema T; Geraedts JP
    J Med Genet; 1987 Jan; 24(1):32-8. PubMed ID: 3806640
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The Martin-Bell syndrome in South Africa.
    Venter PA; Op't Hof J; Coetzee DJ
    Am J Med Genet; 1986; 23(1-2):597-610. PubMed ID: 3953670
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Klinefelter syndrome and two fragile X chromosomes.
    Fryns JP; Kleczkowska A; Wolfs I; van den Berghe H
    Clin Genet; 1984 Nov; 26(5):445-7. PubMed ID: 6499257
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The fragile X syndrome.
    Brown WT
    Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Screening for the fragile X syndrome among the mentally retarded: a clinical study. The Collaborative Fragile X Study Group.
    de Vries BB; Mohkamsing S; van den Ouweland AM; Mol E; Gelsema K; van Rijn M; Tibben A; Halley DJ; Duivenvoorden HJ; Oostra BA; Niermeijer MF
    J Med Genet; 1999 Jun; 36(6):467-70. PubMed ID: 10874635
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The predictive value of dermatoglyphic anomalies in the diagnosis of fra(X)-positive Martin-Bell syndrome (MBS).
    Langenbeck U; Varga I; Hansmann I
    Am J Med Genet; 1988; 30(1-2):169-75. PubMed ID: 3177442
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Chromosomal aberrations in the mildly mentally retarded.
    Göstason R; Wahlström J; Johannisson T; Holmqvist D
    J Ment Defic Res; 1991 Jun; 35 ( Pt 3)():240-6. PubMed ID: 1833552
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Fragile site X chromosomes in mentally retarded boys.
    Moon HR; Moon SY
    J Korean Med Sci; 1993 Jun; 8(3):192-6. PubMed ID: 8240748
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.
    Oberlé I; Heilig R; Moisan JP; Kloepfer C; Mattéi GM; Mattéi JF; Boué J; Froster-Iskenius U; Jacobs PA; Lathrop GM
    Proc Natl Acad Sci U S A; 1986 Feb; 83(4):1016-20. PubMed ID: 3006023
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A systematic cytogenetic study of a population of 1170 mentally retarded and/or behaviourly disturbed patients including fragile X-screening. The Hondsberg experience.
    Schreppers-Tijdink GA; Curfs LM; Wiegers A; Kleczkowska A; Fryns JP
    J Genet Hum; 1988 Dec; 36(5):425-46. PubMed ID: 2975324
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic control over fragile X chromosome expression.
    Hecht F; Fryns JP; Vlietinck RF; Van den Berghe H
    Clin Genet; 1986 Mar; 29(3):191-5. PubMed ID: 3698329
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The marker (X) syndrome: a cytogenetic and genetic analysis.
    Sherman SL; Morton NE; Jacobs PA; Turner G
    Ann Hum Genet; 1984 Jan; 48(1):21-37. PubMed ID: 6712153
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Effect of X inactivation on fragile X frequency and mental retardation.
    Rosenberg C; Vianna-Morgante AM; Otto PA; Navajas L
    Am J Med Genet; 1991; 38(2-3):421-4. PubMed ID: 2018084
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The fragile X syndrome in a large family. I. Cytogenetic and clinical investigations.
    Veenema H; Geraedts JP; Beverstock GC; Pearson PL
    J Med Genet; 1987 Jan; 24(1):23-31. PubMed ID: 3492604
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.