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Journal Abstract Search

154 related items for PubMed ID: 3346020

  • 1. Concurrence of the triple-X syndrome and expression of the fragile site Xq27.3.
    Fuster C, Templado C, Miró R, Barrios L, Egozcue J.
    Hum Genet; 1988 Mar; 78(3):293. PubMed ID: 3346020
    [Abstract] [Full Text] [Related]

  • 2. Fragile site Xq27.3 in a family without mental retardation.
    Romain DR, Chapman CJ.
    Clin Genet; 1992 Jan; 41(1):33-5. PubMed ID: 1633644
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.
    Schmidt M, Certoma A, Du Sart D, Kalitsis P, Leversha M, Fowler K, Sheffield L, Jack I, Danks DM.
    Hum Genet; 1990 Mar; 84(4):347-52. PubMed ID: 2307456
    [Abstract] [Full Text] [Related]

  • 5. [The 47,XXX syndrome in a family with the fragile X chromosome syndrome].
    Seemanová E, Schmidt A, Subrt I, Passarge E, Macek M, Nedomová V.
    Cas Lek Cesk; 1985 Aug 02; 124(31):988-91. PubMed ID: 4028081
    [No Abstract] [Full Text] [Related]

  • 6. Triradial configurations indicate that expression of the fragile site at Xq27 is non-lethal.
    Tommerup N.
    Ann Genet; 1987 Aug 02; 30(4):231-2. PubMed ID: 3501266
    [Abstract] [Full Text] [Related]

  • 7. In situ hybridization studies using a molecular probe that maps to Xq27-Zq28.
    Duncan AM, Morgan C.
    Hum Genet; 1990 Apr 02; 84(5):446-8. PubMed ID: 2323777
    [Abstract] [Full Text] [Related]

  • 8. Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.
    Voelckel MA, Philip N, Piquet C, Pellissier MC, Oberlé I, Birg F, Mattei MG, Mattei JF.
    Hum Genet; 1989 Mar 02; 81(4):353-7. PubMed ID: 2564838
    [Abstract] [Full Text] [Related]

  • 9. The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.
    Veenema H, Carpenter NJ, Bakker E, Hofker MH, Ward AM, Pearson PL.
    J Med Genet; 1987 Jul 02; 24(7):413-21. PubMed ID: 2886667
    [Abstract] [Full Text] [Related]

  • 10. Microdissection of the fragile X region.
    MacKinnon RN, Hirst MC, Bell MV, Watson JE, Claussen U, Ludecke HJ, Senger G, Horsthemke B, Davies KE.
    Am J Hum Genet; 1990 Aug 02; 47(2):181-6. PubMed ID: 2378345
    [Abstract] [Full Text] [Related]

  • 11. Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.
    Blomquist HK, Gustavson KH, Holmgren G, Nordenson I, Pålsson-Stråe U.
    Clin Genet; 1983 Dec 02; 24(6):393-8. PubMed ID: 6652951
    [Abstract] [Full Text] [Related]

  • 12. Pulsed-field gel mapping studies in the vicinity of the fragile site at Xq27.3.
    Patterson M, Bell M, Schwartz C, Davies K.
    Am J Med Genet; 1988 Dec 02; 30(1-2):581-91. PubMed ID: 3177471
    [Abstract] [Full Text] [Related]

  • 13. Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation.
    Voelckel MA, Mattei MG, N'Guyen C, Philip N, Birg F, Mattei JF.
    Hum Genet; 1988 Dec 02; 80(4):375-8. PubMed ID: 2904402
    [Abstract] [Full Text] [Related]

  • 14. Increase in the incidence of the fragile site Xq27 in prometaphases.
    Barbi G, Steinbach P.
    Hum Genet; 1982 Dec 02; 61(1):82. PubMed ID: 6957373
    [No Abstract] [Full Text] [Related]

  • 15. Familial autism and the fragile-X chromosome.
    August GJ, Lockhart LH.
    J Autism Dev Disord; 1984 Jun 02; 14(2):197-204. PubMed ID: 6746507
    [Abstract] [Full Text] [Related]

  • 16. A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation.
    Pembrey ME, Winter RM, Davies KE.
    Am J Med Genet; 1985 Aug 02; 21(4):709-17. PubMed ID: 4040705
    [Abstract] [Full Text] [Related]

  • 17. The fragile X syndrome (Martin-Bell syndrome). Clinical and cytogenetic findings in 16 prepubertal boys and in 4 of their 5 families.
    Schinzel A, Largo RH.
    Helv Paediatr Acta; 1985 Jul 02; 40(2-3):133-52. PubMed ID: 3843245
    [Abstract] [Full Text] [Related]

  • 18. [Clinical, cytogenetic and molecular aspects of fragile X syndrome].
    Veenema H.
    Tijdschr Kindergeneeskd; 1989 Oct 02; 57(5):153-8. PubMed ID: 2683200
    [Abstract] [Full Text] [Related]

  • 19. [Recombination between the fragile site Xq27 and the gene for coagulation factor IX].
    Landoulsi A, de Blois MC, Guérin P, Rethoré MO, Lejeune J, Lucotte G.
    Ann Genet; 1985 Oct 02; 28(4):201-5. PubMed ID: 3879429
    [Abstract] [Full Text] [Related]

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