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84 related items for PubMed ID: 8546149

  • 1. Schizophrenia and the androgen receptor gene: report of a sibship showing co-segregation with Reifenstein syndrome but no evidence for linkage in 23 multiply affected families.
    Arranz M, Sharma T, Sham P, Kerwin R, Nanko S, Owen M, Gill M, Collier D.
    Am J Med Genet; 1995 Oct 09; 60(5):377-81. PubMed ID: 8546149
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  • 2. Failure to find linkage between a functional polymorphism in the dopamine D4 receptor gene and schizophrenia.
    Shaikh S, Gill M, Owen M, Asherson P, McGuffin P, Nanko S, Murray RM, Collier DA.
    Am J Med Genet; 1994 Mar 15; 54(1):8-11. PubMed ID: 8178839
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  • 3. Genetic linkage analysis of schizophrenia using chromosome 11q13-24 markers in Israeli pedigrees.
    Mulcrone J, Whatley SA, Marchbanks R, Wildenauer D, Altmark D, Daoud H, Gur E, Ebstein RP, Lerer B.
    Am J Med Genet; 1995 Apr 24; 60(2):103-8. PubMed ID: 7485242
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  • 4. Further evidence for a susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia by nonparametric linkage analysis.
    Schwab SG, Hallmayer J, Albus M, Lerer B, Hanses C, Kanyas K, Segman R, Borrman M, Dreikorn B, Lichtermann D, Rietschel M, Trixler M, Maier W, Wildenauer DB.
    Am J Med Genet; 1998 Jul 10; 81(4):302-7. PubMed ID: 9674975
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  • 5. Male siblings with schizophrenia share alleles at the androgen receptor above chance expectation.
    Crow TJ, Poulter M, Lofthouse R, Chen G, Shah T, Bass N, Morganti C, Vita A, Smith C, Boccio-Smith A.
    Am J Med Genet; 1993 Oct 15; 48(3):159-60. PubMed ID: 8291571
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  • 6. Potential linkage for schizophrenia on chromosome 22q12-q13: a replication study.
    Schwab SG, Lerer B, Albus M, Maier W, Hallmayer J, Fimmers R, Lichtermann D, Minges J, Bondy B, Ackenheil M.
    Am J Med Genet; 1995 Oct 09; 60(5):436-43. PubMed ID: 8546158
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  • 7. Evaluation of linkage of markers on chromosome 6p with schizophrenia in Taiwanese families.
    Hwu HG, Lin MW, Lee PC, Lee SF, Ou-Yang WC, Liu CM.
    Am J Med Genet; 2000 Feb 07; 96(1):74-8. PubMed ID: 10686556
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  • 8. DNA linkage analysis and studies of the androgen receptor gene in a large kindred with complete androgen insensitivity.
    Imperato-McGinley J, Ip NY, Gautier T, Neuweiler J, Gruenspan H, Liao S, Chang C, Balazs I.
    Am J Med Genet; 1990 May 07; 36(1):104-8. PubMed ID: 2333898
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  • 9. [Familial form of partial androgen insensitivity (Reifenstein syndrome): arginine-histidine mutation in position 840 in the androgen receptor].
    Lumbroso S, Lobaccaro JM, Belon C, Amram S, Rodier M, Bringer J, Sultan C.
    C R Seances Soc Biol Fil; 1993 May 07; 187(4):508-15. PubMed ID: 8019921
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  • 10. Irish study on high-density schizophrenia families: field methods and power to detect linkage.
    Kendler KS, O'Neill FA, Burke J, Murphy B, Duke F, Straub RE, Shinkwin R, Ni Nuallain M, MacLean CJ, Walsh D.
    Am J Med Genet; 1996 Apr 09; 67(2):179-90. PubMed ID: 8723045
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  • 14. A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome.
    Wooster R, Mangion J, Eeles R, Smith S, Dowsett M, Averill D, Barrett-Lee P, Easton DF, Ponder BA, Stratton MR.
    Nat Genet; 1992 Oct 09; 2(2):132-4. PubMed ID: 1303262
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  • 16. Identification of a mutant allele of the androgen receptor gene in a family with androgen insensitivity syndrome: detection of carriers and prenatal diagnosis.
    Fogu G, Bertini V, Dessole S, Bandiera P, Campus PM, Capobianco G, Sanna R, Soro G, Montella A.
    Arch Gynecol Obstet; 2003 Nov 09; 269(1):25-9. PubMed ID: 14605819
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  • 19. Genetic heterogeneity in schizophrenia II: conditional analyses of affected schizophrenia sibling pairs provide evidence for an interaction between markers on chromosome 8p and 14q.
    Chiu YF, McGrath JA, Thornquist MH, Wolyniec PS, Nestadt G, Swartz KL, Lasseter VK, Liang KY, Pulver AE.
    Mol Psychiatry; 2002 Nov 09; 7(6):658-64. PubMed ID: 12140791
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  • 20. Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21.
    Antonarakis SE, Blouin JL, Lasseter VK, Gehrig C, Radhakrishna U, Nestadt G, Housman DE, Kazazian HH, Kalman K, Gutman G, Fantino E, Chandy KG, Gargus JJ, Pulver AE.
    Am J Med Genet; 1999 Aug 20; 88(4):348-51. PubMed ID: 10402501
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