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PUBMED FOR HANDHELDS

Journal Abstract Search


349 related items for PubMed ID: 7182864

  • 21. [Familial mental retardation and the fragile X syndrome].
    Veenema H, Pelckmans AJ, Geraedts JP, Van Leeuwen I, Zvelebil N.
    Tijdschr Kindergeneeskd; 1984 Feb; 52(1):9-15. PubMed ID: 6585033
    [Abstract] [Full Text] [Related]

  • 22. [Mental retardation with X fragility: Armenfrax. Review and personal studies].
    Engel E.
    Rev Med Suisse Romande; 1983 Apr; 103(4):333-44. PubMed ID: 6348915
    [No Abstract] [Full Text] [Related]

  • 23. X-linked mental retardation with the fragile X. A study of 15 families.
    Mattei JF, Mattei MG, Aumeras C, Auger M, Giraud F.
    Hum Genet; 1981 Apr; 59(4):281-9. PubMed ID: 7333582
    [Abstract] [Full Text] [Related]

  • 24. Fragile X syndrome: a unique mutation in man.
    Nussbaum RL, Ledbetter DH.
    Annu Rev Genet; 1986 Apr; 20():109-45. PubMed ID: 3545058
    [No Abstract] [Full Text] [Related]

  • 25. A father and daughter with fragile X chromosome.
    Morić-Petrović S, Laća Z.
    J Med Genet; 1983 Dec; 20(6):476. PubMed ID: 6655679
    [No Abstract] [Full Text] [Related]

  • 26. No significant relationship between age and frequency of chromosome lesions in mentally retarded individuals with or without the fragile X syndrome.
    Butler MG.
    Hum Genet; 1990 Jan; 84(2):216-7. PubMed ID: 2298460
    [No Abstract] [Full Text] [Related]

  • 27. Two brothers with mental retardation discordant for the fragile-X syndrome.
    Van Roy BC, Willems PJ, Vits LJ, Ceulemans BP, Coucke PJ, Van der Auwera BJ, Lormans JA, Dumon JE.
    Am J Med Genet; 1990 May; 36(1):122-5. PubMed ID: 2333901
    [Abstract] [Full Text] [Related]

  • 28. A marker X chromosome associated with nonspecific male mental retardation. The first South African cases.
    Venter PA, Gericke GS, Dawson B, Op't Hof J.
    S Afr Med J; 1981 Nov 21; 60(21):807-11. PubMed ID: 7302747
    [Abstract] [Full Text] [Related]

  • 29. Frequency of the fragile X syndrome in Japanese mentally retarded males.
    Arinami T, Kondo I, Nakajima S.
    Hum Genet; 1986 Aug 21; 73(4):309-12. PubMed ID: 3744362
    [Abstract] [Full Text] [Related]

  • 30. 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 21; 84(4):347-52. PubMed ID: 2307456
    [Abstract] [Full Text] [Related]

  • 31. Fragile X chromosome in institutionalized male adults with mental retardation.
    Aoi T, Takashima H, Takada T, Okada T.
    Keio J Med; 1989 Mar 21; 38(1):36-9. PubMed ID: 2785613
    [Abstract] [Full Text] [Related]

  • 32. [Mental deficiency associated with a fragility of the X chromosome].
    Guitart Feliubadalo M, Artigas Pallarés J, Fuster Marqués C, Gabau Vila E, Lorente Hurtado I, Argemí Renom J.
    An Esp Pediatr; 1988 Nov 21; 29(5):377-81. PubMed ID: 3232895
    [Abstract] [Full Text] [Related]

  • 33. Prevalence of fragile X-chromosome.
    Lancet; 1984 Jan 28; 1(8370):220-1. PubMed ID: 6141356
    [No Abstract] [Full Text] [Related]

  • 34. [[Incidence of X-chromosome fragility in medium and severe mental retardation].
    Szakmáry E, Tomsits E, Vass M, Schuler D.
    Orv Hetil; 1984 May 13; 125(20):1195-9. PubMed ID: 6718007
    [No Abstract] [Full Text] [Related]

  • 35. [Mental retardation linked to fragility of chromosome X: current knowledge].
    Mattei JF, Mattei MG, Auger M, Giraud F.
    J Genet Hum; 1984 Jul 13; 32(3):167-92. PubMed ID: 6237176
    [Abstract] [Full Text] [Related]

  • 36. The fragile X syndrome: first family reported in Malaysia.
    Ten SK, Chin YM, Jamilatul Noor MB, Hassan K.
    Singapore Med J; 1985 Jul 13; 26(4-5):372-8. PubMed ID: 4071092
    [No Abstract] [Full Text] [Related]

  • 37. Fragile X-linked mental retardation: the Martin-Bell syndrome.
    Richards BW, Sylvester PE, Brooker C.
    J Ment Defic Res; 1981 Dec 13; 25 Pt 4():253-6. PubMed ID: 7328634
    [Abstract] [Full Text] [Related]

  • 38. Molecular diagnosis of fragile X syndrome using methylation sensitive techniques in a cohort of patients with intellectual disability.
    Chaudhary AG, Hussein IR, Abuzenadah A, Gari M, Bassiouni R, Sogaty S, Lary S, Al-Quaiti M, Al Balwi M, Al Qahtani M.
    Pediatr Neurol; 2014 Apr 13; 50(4):368-76. PubMed ID: 24630283
    [Abstract] [Full Text] [Related]

  • 39. Cytogenetic survey for autistic fragile X carriers in a mental retardation center.
    Cantú ES, Stone JW, Wing AA, Langee HR, Williams CA.
    Am J Ment Retard; 1990 Jan 13; 94(4):442-7. PubMed ID: 2297426
    [Abstract] [Full Text] [Related]

  • 40. The fragile X marker and autism in perspective.
    Payton JB, Steele MW, Wenger SL, Minshew NJ.
    J Am Acad Child Adolesc Psychiatry; 1989 May 13; 28(3):417-21. PubMed ID: 2738009
    [Abstract] [Full Text] [Related]


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