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Journal Abstract Search

354 related items for PubMed ID: 9222959

  • 21. Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21.
    Häne B, Schroer RJ, Arena JF, Lubs HA, Schwartz CE, Stevenson RE.
    Clin Genet; 1996 Oct; 50(4):176-83. PubMed ID: 9001795
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  • 22. MASA syndrome: new clinical features and linkage analysis using DNA probes.
    Schrander-Stumpel C, Legius E, Fryns JP, Cassiman JJ.
    J Med Genet; 1990 Nov; 27(11):688-92. PubMed ID: 2277384
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  • 24. Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: linkage analysis and clinical findings in a three-generation Sardinian family.
    Russo S, Cogliati F, Cavalleri F, Cassitto MG, Giglioli R, Toniolo D, Casari G, Larizza L.
    Am J Med Genet; 2000 Oct 23; 94(5):376-82. PubMed ID: 11050621
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  • 26. Allan-Herndon syndrome. I. Clinical studies.
    Stevenson RE, Goodman HO, Schwartz CE, Simensen RJ, McLean WT, Herndon CN.
    Am J Hum Genet; 1990 Sep 23; 47(3):446-53. PubMed ID: 2393019
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  • 27. X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28.
    Armfield K, Nelson R, Lubs HA, Häne B, Schroer RJ, Arena F, Schwartz CE, Stevenson RE.
    Am J Med Genet; 1999 Jul 30; 85(3):236-42. PubMed ID: 10398235
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  • 28. A new X linked syndrome with mental retardation and craniofacial dysmorphism?
    Hyde-Forster I, McCarthy G, Berry AC.
    J Med Genet; 1992 Oct 30; 29(10):736-8. PubMed ID: 1433236
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  • 30. Nonsyndromic X-linked mental retardation: mapping of MRX58 to the pericentromeric region.
    Holinski-Feder E, Chahrockh-Zadeh S, Rittinger O, Jedele KB, Gasteiger M, Lenski C, Murken J, Golla A.
    Am J Med Genet; 1999 Sep 10; 86(2):102-6. PubMed ID: 10449641
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  • 31. Spectrum of X-linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): Clinical review with six additional families.
    Schrander-Stumpel C, Höweler C, Jones M, Sommer A, Stevens C, Tinschert S, Israel J, Fryns JP.
    Am J Med Genet; 1995 May 22; 57(1):107-16. PubMed ID: 7645588
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  • 32. A new X linked mental retardation (XLMR) syndrome with short stature, small testes, muscle wasting, and tremor localises to Xq24-q25.
    Cabezas DA, Slaugh R, Abidi F, Arena JF, Stevenson RE, Schwartz CE, Lubs HA.
    J Med Genet; 2000 Sep 22; 37(9):663-8. PubMed ID: 10978355
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  • 33. Genotype-phenotype correlation in L1 associated diseases.
    Fransen E, Van Camp G, D'Hooge R, Vits L, Willems PJ.
    J Med Genet; 1998 May 22; 35(5):399-404. PubMed ID: 9610803
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  • 36. Genetic heterogeneity of FG syndrome: a fourth locus (FGS4) maps to Xp11.4-p11.3 in an Italian family.
    Piluso G, Carella M, D'Avanzo M, Santinelli R, Carrano EM, D'Avanzo A, D'Adamo AP, Gasparini P, Nigro V.
    Hum Genet; 2003 Feb 22; 112(2):124-30. PubMed ID: 12522552
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  • 37. Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28.
    Biancalana V, Le Marec B, Odent S, van den Hurk JA, Hanauer A.
    Hum Genet; 1991 Dec 22; 88(2):228-30. PubMed ID: 1757098
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