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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

105 related items for PubMed ID: 8882866

  • 1. Localization of the gene (or genes) for a syndrome with X-linked mental retardation, ataxia, weakness, hearing impairment, loss of vision and a fatal course in early childhood.
    Kremer H, Hamel BC, van den Helm B, Arts WF, de Wijs IJ, Sistermans EA, Ropers HH, Mariman EC.
    Hum Genet; 1996 Nov; 98(5):513-7. PubMed ID: 8882866
    [Abstract] [Full Text] [Related]

  • 2. A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
    Tranebjaerg L, Schwartz C, Eriksen H, Andreasson S, Ponjavic V, Dahl A, Stevenson RE, May M, Arena F, Barker D.
    J Med Genet; 1995 Apr; 32(4):257-63. PubMed ID: 7643352
    [Abstract] [Full Text] [Related]

  • 3. X-linked ataxia, weakness, deafness, and loss of vision in early childhood with a fatal course.
    Arts WF, Loonen MC, Sengers RC, Slooff JL.
    Ann Neurol; 1993 May; 33(5):535-9. PubMed ID: 8498830
    [Abstract] [Full Text] [Related]

  • 4. Localization of a non-specific X-linked mental retardation gene, MRX23, to Xq23-q24.
    Gregg RG, Palmer C, Kirkpatrick S, Simantel A.
    Hum Mol Genet; 1996 Mar; 5(3):411-4. PubMed ID: 8852668
    [Abstract] [Full Text] [Related]

  • 5. Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).
    Gu XX, Decorte R, Marynen P, Fryns JP, Cassiman JJ, Raeymaekers P.
    J Med Genet; 1996 Jan; 33(1):52-5. PubMed ID: 8825049
    [Abstract] [Full Text] [Related]

  • 6. Linkage of nonspecific X-linked mental retardation to Xq21.31.
    Jedele KB, Michels VV, Schaid DJ, Schowalter KV, Thibodeau SN.
    Am J Med Genet; 1996 Jan; 43(1-2):436-42. PubMed ID: 1605223
    [Abstract] [Full Text] [Related]

  • 7. Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21.
    Bach I, Robinson D, Thomas N, Ropers HH, Cremers FP.
    Hum Genet; 1992 Aug; 89(6):620-4. PubMed ID: 1511979
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Linkage mapping of a severe X-linked mental retardation syndrome.
    Malmgren H, Sundvall M, Dahl N, Gustavson KH, Annerén G, Wadelius C, Steén-Bondeson ML, Pettersson U.
    Am J Hum Genet; 1993 Jun; 52(6):1046-52. PubMed ID: 8503440
    [Abstract] [Full Text] [Related]

  • 10. Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter.
    Dlouhy SR, Christian JC, Haines JL, Conneally PM, Hodes ME.
    Hum Genet; 1987 Feb; 75(2):136-9. PubMed ID: 3469136
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. X-linked mental retardation with dystonic movements of the hands.
    Partington MW, Mulley JC, Sutherland GR, Hockey A, Thode A, Turner G.
    Am J Med Genet; 1988 Feb; 30(1-2):251-62. PubMed ID: 3177452
    [Abstract] [Full Text] [Related]

  • 13. Clasped-thumb mental retardation (MASA) syndrome: confirmation of linkage to Xq28.
    Macias VR, Day DW, King TE, Wilson GN.
    Am J Med Genet; 1988 Feb; 43(1-2):408-14. PubMed ID: 1605219
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Localisation of the MRX3 gene for non-specific X linked mental retardation.
    Gedeon A, Kerr B, Mulley J, Turner G.
    J Med Genet; 1991 Jun; 28(6):372-7. PubMed ID: 1870093
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Molecular analysis of four males with mental retardation and deletions of Xq21 places the putative MR region in Xq21.1 between DXS233 and CHM.
    May M, Colleaux L, Murgia A, Aylsworth A, Nussbaum R, Fontes M, Schwartz C.
    Hum Mol Genet; 1995 Aug; 4(8):1465-6. PubMed ID: 7581391
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.