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Journal Abstract Search

122 related items for PubMed ID: 3177453

  • 21. The strength of association between fragile (X) chromosome presence and mental retardation.
    Silverman W, Lubin R, Jenkins EC, Brown WT.
    Clin Genet; 1983 Jun; 23(6):436-40. PubMed ID: 6684008
    [Abstract] [Full Text] [Related]

  • 22. A recognizable syndrome of sex-linked mental retardation, large testes, and marker X chromosome.
    Hecht JT, Moore CM, Scott CI.
    South Med J; 1981 Dec; 74(12):1493-6. PubMed ID: 6947439
    [No Abstract] [Full Text] [Related]

  • 23. X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriers.
    Nielsen KB, Tommerup N, Poulsen H, Mikkelsen M.
    Hum Genet; 1981 Dec; 59(1):23-5. PubMed ID: 10819017
    [Abstract] [Full Text] [Related]

  • 24. Linkage of nonspecific X-linked mental retardation to Xq21.31.
    Jedele KB, Michels VV, Schaid DJ, Schowalter KV, Thibodeau SN.
    Am J Med Genet; 1981 Dec; 43(1-2):436-42. PubMed ID: 1605223
    [Abstract] [Full Text] [Related]

  • 25. MRX8: an X-linked mental retardation condition with linkage to Xq21.
    Schwartz CE, May M, Huang T, Ledbetter D, Anderson G, Barker DF, Lubs HA, Arena F, Stevenson RE.
    Am J Med Genet; 1981 Dec; 43(1-2):467-74. PubMed ID: 1605227
    [Abstract] [Full Text] [Related]

  • 26. Fragile (X)(q27) sites in a pedigree with female carriers showing mild to severe mental retardation.
    Webb GC, Halliday JL, Pitt DB, Judge CG, Leversha M.
    J Med Genet; 1982 Feb; 19(1):44-8. PubMed ID: 7069746
    [Abstract] [Full Text] [Related]

  • 27. Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2).
    Sutherland GR, Gedeon AK, Haan EA, Woodroffe P, Mulley JC.
    Am J Med Genet; 1988 Feb; 30(1-2):493-508. PubMed ID: 3177467
    [Abstract] [Full Text] [Related]

  • 28. 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]

  • 29. Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletion.
    Hodgson SV, Robertson ME, Fear CN, Goodship J, Malcolm S, Jay B, Bobrow M, Pembrey ME.
    Hum Genet; 1987 Mar; 75(3):286-90. PubMed ID: 3030927
    [Abstract] [Full Text] [Related]

  • 30. Spastic paraplegia with iron deposits in the basal ganglia: a new X-linked mental retardation syndrome.
    Arena JF, Schwartz C, Stevenson R, Lawrence L, Carpenter A, Duara R, Ledbetter D, Huang T, Lehner T, Ott J.
    Am J Med Genet; 1987 Mar; 43(1-2):479-90. PubMed ID: 1605230
    [Abstract] [Full Text] [Related]

  • 31. Alpha thalassaemia/mental retardation syndrome (non-deletional type): report of a family supporting X linked inheritance.
    Cole TR, May A, Hughes HE.
    J Med Genet; 1991 Nov; 28(11):734-7. PubMed ID: 1770528
    [Abstract] [Full Text] [Related]

  • 32. Possible erasure of the imprint on a fragile X chromosome when transmitted by a male.
    Laird CD.
    Am J Med Genet; 1991 Nov; 38(2-3):391-5. PubMed ID: 2018078
    [Abstract] [Full Text] [Related]

  • 33. Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male.
    Camerino G, Mattei MG, Mattei JF, Jaye M, Mandel JL.
    Nature; 1991 Nov; 306(5944):701-4. PubMed ID: 6689201
    [Abstract] [Full Text] [Related]

  • 34. Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22.
    des Portes V, Pinard JM, Smadja D, Motte J, Boespflüg-Tanguy O, Moutard ML, Desguerre I, Billuart P, Carrie A, Bienvenu T, Vinet MC, Bachner L, Beldjord C, Dulac O, Kahn A, Ponsot G, Chelly J.
    J Med Genet; 1997 Mar; 34(3):177-83. PubMed ID: 9132485
    [Abstract] [Full Text] [Related]

  • 35. On the genetics of Rett syndrome: analysis of family and pedigree data.
    Killian W.
    Am J Med Genet Suppl; 1986 Mar; 1():369-76. PubMed ID: 3087198
    [Abstract] [Full Text] [Related]

  • 36. Marker X-associated mental retardation. A study of 150 retarded males.
    Kähkönen M, Leisti J, Wilska M, Varonen S.
    Clin Genet; 1983 Jun; 23(6):397-404. PubMed ID: 6576874
    [Abstract] [Full Text] [Related]

  • 37. 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]

  • 38. A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14.
    Suthers GK, Turner G, Mulley JC.
    Am J Med Genet; 1988 Nov; 30(1-2):485-91. PubMed ID: 3177466
    [Abstract] [Full Text] [Related]

  • 39. A study of mental retardation in children in the Island of Hawaii.
    Proops R, Mayer M, Jacobs PA.
    Clin Genet; 1983 Feb; 23(2):81-96. PubMed ID: 6839531
    [Abstract] [Full Text] [Related]

  • 40. Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3.
    Kozák L, Chiurazzi P, Genuardi M, Pomponi MG, Zollino M, Neri G.
    J Med Genet; 1993 Oct; 30(10):866-9. PubMed ID: 8230164
    [Abstract] [Full Text] [Related]

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