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

195 related items for PubMed ID: 8503437

  • 1. X-linked mental retardation: in pursuit of a gene map.
    Schwartz CE.
    Am J Hum Genet; 1993 Jun; 52(6):1025-31. PubMed ID: 8503437
    [No Abstract] [Full Text] [Related]

  • 2. Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.
    Strain L, Wright AF, Bonthron DT.
    J Med Genet; 1997 Jul; 34(7):535-40. PubMed ID: 9222959
    [Abstract] [Full Text] [Related]

  • 3. A new X linked syndrome with mental retardation and craniofacial dysmorphism?
    Hyde-Forster I, McCarthy G, Berry AC.
    J Med Genet; 1992 Oct; 29(10):736-8. PubMed ID: 1433236
    [Abstract] [Full Text] [Related]

  • 4. X-linked dysmorphic syndrome with mental retardation.
    Prieto F, Badía L, Mulas F, Monfort A, Mora F.
    Clin Genet; 1987 Nov; 32(5):326-34. PubMed ID: 3121220
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21).
    Saugier-Veber P, Abadie V, Moncla A, Mathieu M, Piussan C, Turleau C, Mattei JF, Munnich A, Lyonnet S.
    Am J Hum Genet; 1993 Jun; 52(6):1040-5. PubMed ID: 8503439
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. 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]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Gene localization in a family with X-linked syndromal mental retardation (Prieto syndrome).
    Watty A, Prieto F, Beneyto M, Neugebauer M, Gal A.
    Am J Med Genet; 1991 Feb; 38(2-3):234-9. PubMed ID: 1673297
    [Abstract] [Full Text] [Related]

  • 14. Familial X-linked mental retardation and fragile X chromosomes in two Swedish families.
    Gustavson KH, Holmgren G, Blomquist HK, Mikkelsen M, Nordenson I, Poulsen H, Tommerup N.
    Clin Genet; 1981 Feb; 19(2):101-10. PubMed ID: 7193540
    [Abstract] [Full Text] [Related]

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

  • 16. XLMR genes: update 1992.
    Neri G, Chiurazzi P, Arena F, Lubs HA, Glass IA.
    Am J Med Genet; 1981 Feb; 43(1-2):373-82. PubMed ID: 1605215
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Fine mapping of X-linked clasped thumb and mental retardation (MASA syndrome) in Xq28.
    Legius E, Kaepernick L, Higgins JV, Glover TW.
    Clin Genet; 1994 Apr; 45(4):165-8. PubMed ID: 8062432
    [Abstract] [Full Text] [Related]

  • 19. A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.
    Shashi V, Berry MN, Shoaf S, Sciote JJ, Goldstein D, Hart TC.
    Am J Hum Genet; 2000 Feb; 66(2):469-79. PubMed ID: 10677307
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.