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Journal Abstract Search

151 related items for PubMed ID: 10190484

  • 1. Evidence for a new X-linked mental retardation gene in Xp21-Xp22: clinical and molecular data in one family.
    Ronce N, Raynaud M, Toutain A, Moizard MP, Colleaux L, Gendrot C, Briault S, Moraine C.
    Am J Med Genet; 1999 Mar 12; 83(2):132-7. PubMed ID: 10190484
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  • 2. Regional localization of an X-linked mental retardation gene to Xp21.1-Xp22.13 (MRX38).
    Schutz CK, Ives EJ, Chalifoux M, MacLaren L, Farrell S, Robinson PD, White BN, Holden JJ.
    Am J Med Genet; 1996 Jul 12; 64(1):89-96. PubMed ID: 8826457
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  • 3. Regional localization of a nonspecific X-linked mental retardation gene (MRX59) to Xp21.2-p22.2.
    Carpenter NJ, Brown WT, Qu Y, Keenan KL.
    Am J Med Genet; 1999 Jul 30; 85(3):266-70. PubMed ID: 10398241
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  • 5. Gene for apparently nonsyndromic X-linked mental retardation (MRX32) maps to an 18-Mb region of Xp21.2-p22.
    Häne B, Stevenson RE, Arena JF, Lubs HA, Simensen RJ, Schwartz CE.
    Am J Med Genet; 1999 Jul 30; 85(3):271-5. PubMed ID: 10398242
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  • 6. 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; 30(10):866-9. PubMed ID: 8230164
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  • 8. Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysis.
    Hanauer A, Alembik Y, Gilgenkrantz S, Mujica P, Nivelon-Chevallier A, Pembrey ME, Young ID, Mandel JL.
    Am J Med Genet; 1988 Oct 30; 30(1-2):523-30. PubMed ID: 3177469
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  • 9. Linkage analysis suggests at least two loci for X-linked non-specific mental retardation.
    Arveiler B, Alembik Y, Hanauer A, Jacobs P, Tranebjaerg L, Mikkelsen M, Puissant H, Piet LL, Mandel JL.
    Am J Med Genet; 1988 Oct 30; 30(1-2):473-83. PubMed ID: 3177465
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  • 11. Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54).
    Jemaa LB, des Portes V, Zemni R, Mrad R, Maazoul F, Beldjord C, Chaabouni H, Chelly J.
    Am J Med Genet; 1999 Jul 30; 85(3):276-82. PubMed ID: 10398243
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  • 14. Gene for non-specific X-linked mental retardation maps in the pericentromeric region.
    Samanns C, Albrecht R, Neugebauer M, Neri G, Gal A.
    Am J Med Genet; 1991 Jul 30; 38(2-3):224-7. PubMed ID: 2018062
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  • 15. A second family with nonsyndromic sensorineural hearing loss linked to Xp21.2: refinement of the DFN4 locus within DMD.
    Pfister MH, Apaydin F, Turan O, Bereketoglu M, Bylgen V, Braendle U, Zenner HP, Lalwani AK.
    Genomics; 1998 Nov 01; 53(3):377-82. PubMed ID: 9799605
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  • 16. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.
    Towbin JA, Hejtmancik JF, Brink P, Gelb B, Zhu XM, Chamberlain JS, McCabe ER, Swift M.
    Circulation; 1993 Jun 01; 87(6):1854-65. PubMed ID: 8504498
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  • 17. 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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  • 18. 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 10; 45(3):145-53. PubMed ID: 8026106
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  • 19. Confirmation of linkage in X-linked infantile spasms (West syndrome) and refinement of the disease locus to Xp21.3-Xp22.1.
    Bruyere H, Lewis S, Wood S, MacLeod PJ, Langlois S.
    Clin Genet; 1999 Mar 10; 55(3):173-81. PubMed ID: 10334471
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