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Journal Abstract Search

122 related items for PubMed ID: 3177453

  • 41.
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  • 42. Nonspecific X-linked mental retardation--a review.
    Tariverdian G, Weck B.
    Hum Genet; 1982; 62(2):95-109. PubMed ID: 6761264
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  • 46. Clasped-thumb mental retardation (MASA) syndrome: confirmation of linkage to Xq28.
    Macias VR, Day DW, King TE, Wilson GN.
    Am J Med Genet; 1982; 43(1-2):408-14. PubMed ID: 1605219
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  • 47. 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
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  • 48. Linkage to Xq28 in a family with nonspecific X-linked mental retardation.
    Nordström AM, Penttinen M, von Koskull H.
    Hum Genet; 1992 Nov; 90(3):263-6. PubMed ID: 1362558
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  • 49. Familial X-linked mental retardation, verbal disability, and marker X chromosomes.
    Howard-Peebles PN, Stoddard GR, Mims MG.
    Am J Hum Genet; 1979 Mar; 31(2):214-22. PubMed ID: 453204
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  • 52. 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
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  • 53. Mental retardation, acromegalic face, and megalotestes in two half-brothers: a specific form of X-linked mental retardation without fra(X) (q)?
    Tariverdian G, Froster-Iskenius U, Deuschl G, Wolff G.
    Am J Med Genet; 1991 Oct; 38(2-3):208-11. PubMed ID: 2018059
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  • 55. X-linked mental retardation, growth retardation, deafness and microgenitalism. A second familial report.
    Mattei JF, Collignon P, Ayme S, Giraud F.
    Clin Genet; 1983 Jan; 23(1):70-4. PubMed ID: 6682021
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  • 57. Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qter.
    Gregg RG, Metzenberg AB, Hogan K, Sekhon G, Laxova R.
    Genomics; 1991 Apr; 9(4):701-6. PubMed ID: 1674730
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  • 58. Non-specific X linked mental retardation with aphasia exhibiting genetic linkage to chromosomal region Xp11.
    Wilson GN, Richards CS, Katz K, Brookshire GS.
    J Med Genet; 1992 Sep; 29(9):629-34. PubMed ID: 1357179
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  • 59. Coffin-Lowry syndrome: a multicenter study.
    Gilgenkrantz S, Mujica P, Gruet P, Tridon P, Schweitzer F, Nivelon-Chevallier A, Nivelon JL, Couillault G, David A, Verloes A.
    Clin Genet; 1988 Oct; 34(4):230-45. PubMed ID: 3069251
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  • 60. X-linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric region.
    Gendrot C, Ronce N, Toutain A, Moizard MP, Müh JP, Raynaud M, Dourlens J, Briault S, Moraine C.
    Clin Genet; 1994 Mar; 45(3):145-53. PubMed ID: 8026106
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