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 *

127 related articles for article (PubMed ID: 3953660)

  • 1. Fragile X chromosome frequency is consistent temporally and within replicate cultures.
    Jenkins EC; Kastin BR; Krawczun MS; Lele KP; Silverman WP; Brown WT
    Am J Med Genet; 1986; 23(1-2):475-81. PubMed ID: 3953660
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fragile X expression increased by low cell-culture density.
    Krawczun MS; Lele KP; Jenkins EC; Brown WT
    Am J Med Genet; 1986; 23(1-2):467-73. PubMed ID: 2937301
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Spontaneous and induced chromosome instability in patients with fragile X syndrome].
    Suleĭmanova DG; Kuleshov NP
    Genetika; 1987 Mar; 23(3):504-9. PubMed ID: 3569895
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Frequency of tri- or multiradial configurations in fragile X identification.
    Jenkins EC; Duncan CJ; Krawczun MS; Berns LM; Sanz MM; Brown WT
    Am J Med Genet; 1986; 23(1-2):531-5. PubMed ID: 2937304
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Constitutive fragile sites in fra(X) individuals.
    Jenkins EC; Lele KP; Krawczun MS; Gross AC; Duncan CJ; Brown WT
    Am J Med Genet; 1988; 30(1-2):429-34. PubMed ID: 3052066
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. A fragile X suppressor in the normal human blood?
    Soudek D; Emanuel M
    Hum Genet; 1983; 65(1):88-9. PubMed ID: 6642512
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fragile X expression in short-term whole blood cultures is affected by cell density.
    Krawczun MS; Jenkins EC; Brown WT; Silverman WP
    Am J Med Genet; 1988; 30(1-2):435-42. PubMed ID: 2972206
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fragile (X) X-linked mental retardation. II. Frequency and replication pattern of fragile (X)(q28) in heterozygotes.
    Knoll JH; Chudley AE; Gerrard JW
    Am J Hum Genet; 1984 May; 36(3):640-5. PubMed ID: 6731439
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromosome studies in 10 patients with the Rett syndrome.
    Moore JW; Tuck-Muller CM; Murphy M; Naidu S; Thomas GH
    Am J Med Genet Suppl; 1986; 1():345-54. PubMed ID: 3087195
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A comparison of fragile X expression in lymphocyte and lymphoblastoid cultures.
    Abruzzo MA; Hunt PA; Mayer M; Jacobs PA; Wang JC; Erbe RW
    Am J Hum Genet; 1986 Apr; 38(4):533-9. PubMed ID: 3706301
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multilocus analysis of the fragile X syndrome.
    Brown WT; Gross A; Chan C; Jenkins EC; Mandel JL; Oberlé I; Arveiler B; Novelli G; Thibodeau S; Hagerman R
    Hum Genet; 1988 Mar; 78(3):201-5. PubMed ID: 3162224
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of sister chromatid exchanges in fra (X) individuals.
    Gregory P; Wang N; Howard-Peebles PN
    Am J Med Genet; 1986; 23(1-2):563-6. PubMed ID: 3513571
    [No Abstract]   [Full Text] [Related]  

  • 15. Fragile X syndrome in Japanese patients with infantile autism.
    Matsuishi T; Shiotsuki Y; Niikawa N; Katafuchi Y; Otaki E; Ando H; Yamashita Y; Horikawa M; Urabe F; Kuriya N
    Pediatr Neurol; 1987; 3(5):284-7. PubMed ID: 3334020
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Carrier detection and X-inactivation studies in the fragile X syndrome. Cytogenetic studies in 63 obligate and potential carriers of the fragile X.
    Nielsen KB; Tommerup N; Poulsen H; Jacobsen P; Beck B; Mikkelsen M
    Hum Genet; 1983; 64(3):240-5. PubMed ID: 6885068
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The combined effects of FUdR addition and methionine depletion on the X-chromosome fragile site.
    Glover TW; Howard-Peebles PN
    Am J Hum Genet; 1983 Jan; 35(1):117-22. PubMed ID: 6218753
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Further evidence for genetic heterogeneity in the fragile X syndrome.
    Brown WT; Jenkins EC; Gross AC; Chan CB; Krawczun MS; Duncan CJ; Sklower SL; Fisch GS
    Hum Genet; 1987 Apr; 75(4):311-21. PubMed ID: 2883105
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Demonstration of the fra(X) in lymphocytes, fibroblasts, and bone marrow in a patient with a testicular tumour.
    Del Pozo BC; Millard PR
    J Med Genet; 1983 Jun; 20(3):225-7. PubMed ID: 6876116
    [TBL] [Abstract][Full Text] [Related]  

  • 20. In situ nick translation of the fragile X region.
    Nolin SL; Jenkins EC; Brown WT; Dobkin CS
    Am J Med Genet; 1988; 30(1-2):443-50. PubMed ID: 3052067
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.