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160 related items for PubMed ID: 1673297

  • 1. 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; 38(2-3):234-9. PubMed ID: 1673297
    [Abstract] [Full Text] [Related]

  • 2. 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; 38(2-3):224-7. PubMed ID: 2018062
    [Abstract] [Full Text] [Related]

  • 3. X-linked mental retardation syndrome with characteristic "coarse" facial appearance, brachydactyly, and short stature maps to proximal Xq.
    Carpenter NJ, Qu Y, Curtis M, Patil SR.
    Am J Med Genet; 1999 Jul 30; 85(3):230-5. PubMed ID: 10398234
    [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 30; 32(5):326-34. PubMed ID: 3121220
    [Abstract] [Full Text] [Related]

  • 5. 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 30; 45(3):145-53. PubMed ID: 8026106
    [Abstract] [Full Text] [Related]

  • 6. Pericentromeric genes for non-specific X-linked mental retardation (MRX).
    Gedeon A, Kerr B, Mulley J, Turner G.
    Am J Med Genet; 1994 Jul 15; 51(4):553-64. PubMed ID: 7943039
    [Abstract] [Full Text] [Related]

  • 7. Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis.
    Musarella MA, Burghes A, Anson-Cartwright L, Mahtani MM, Argonza R, Tsui LC, Worton R.
    Am J Hum Genet; 1988 Oct 15; 43(4):484-94. PubMed ID: 2902787
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 29(9):629-34. PubMed ID: 1357179
    [Abstract] [Full Text] [Related]

  • 9. 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 Sep 15; 30(1-2):485-91. PubMed ID: 3177466
    [Abstract] [Full Text] [Related]

  • 10. Genetic mapping of loci for X-linked retinitis pigmentosa.
    Dahl N, Sundvall M, Pettersson U, Andréasson S, Anvret M, Kugelberg U, Hagbyhn-Gericke A, Goonewardena P.
    Clin Genet; 1991 Dec 15; 40(6):435-40. PubMed ID: 1685699
    [Abstract] [Full Text] [Related]

  • 11. Renpenning syndrome maps to Xp11.
    Stevenson RE, Arena JF, Ouzts E, Gibson A, Shokeir MH, Vnencak-Jones C, Lubs HA, May M, Schwartz CE.
    Am J Hum Genet; 1998 May 15; 62(5):1092-101. PubMed ID: 9545405
    [Abstract] [Full Text] [Related]

  • 12. Nance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysis.
    Stambolian D, Lewis RA, Buetow K, Bond A, Nussbaum R.
    Am J Hum Genet; 1990 Jul 15; 47(1):13-9. PubMed ID: 1971992
    [Abstract] [Full Text] [Related]

  • 13. Linkage analysis in a large family with nonspecific X-linked mental retardation.
    Glass IA, White EM, Pope MJ, Pirrit LA, Cockburn F, Connor JM.
    Am J Med Genet; 1991 Jul 15; 38(2-3):240-3. PubMed ID: 1673298
    [Abstract] [Full Text] [Related]

  • 14. Localization of the X-linked retinitis pigmentosa locus between DXS7 and DXS84 in a family showing tapetal reflex in heterozygotes.
    Chen JD, Halliday F, Serravalle S, Denton M.
    Ophthalmic Paediatr Genet; 1988 Nov 15; 9(3):143-7. PubMed ID: 2906743
    [Abstract] [Full Text] [Related]

  • 15. Localization of the gene for Wieacker-Wolff syndrome in the pericentromeric region of the X chromosome.
    Kloos DU, Jakubiczka S, Wienker T, Wolff G, Wieacker P.
    Hum Genet; 1997 Sep 15; 100(3-4):426-30. PubMed ID: 9272167
    [Abstract] [Full Text] [Related]

  • 16. Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?
    Passos-Bueno MR, Byth BC, Rosenberg S, Takata RI, Bakker E, Beggs AH, Pavanello RC, Vainzof M, Davies KE, Zatz M.
    Am J Med Genet; 1993 Apr 15; 46(2):172-5. PubMed ID: 8484404
    [Abstract] [Full Text] [Related]

  • 17. 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 15; 30(10):866-9. PubMed ID: 8230164
    [Abstract] [Full Text] [Related]

  • 18. Linkage mapping of a severe X-linked mental retardation syndrome.
    Malmgren H, Sundvall M, Dahl N, Gustavson KH, Annerén G, Wadelius C, Steén-Bondeson ML, Pettersson U.
    Am J Hum Genet; 1993 Jun 15; 52(6):1046-52. PubMed ID: 8503440
    [Abstract] [Full Text] [Related]

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  • 20. Localization of non-specific X-linked mental retardation genes.
    Kerr B, Gedeon A, Mulley J, Turner G.
    Am J Med Genet; 1993 Jun 15; 43(1-2):392-401. PubMed ID: 1605217
    [Abstract] [Full Text] [Related]

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