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Journal Abstract Search

117 related items for PubMed ID: 7663516

  • 1. Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1.
    Figuera LE, Pandolfo M, Dunne PW, Cantú JM, Patel PI.
    Nat Genet; 1995 Jun; 10(2):202-7. PubMed ID: 7663516
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  • 2. Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X-linked trait.
    Tadin-Strapps M, Salas-Alanis JC, Moreno L, Warburton D, Martinez-Mir A, Christiano AM.
    Clin Genet; 2003 May; 63(5):418-22. PubMed ID: 12752576
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  • 3. Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1.
    Casey B, Devoto M, Jones KL, Ballabio A.
    Nat Genet; 1993 Dec; 5(4):403-7. PubMed ID: 8298651
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  • 5. A locus for axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26.
    Priest JM, Fischbeck KH, Nouri N, Keats BJ.
    Genomics; 1995 Sep 20; 29(2):409-12. PubMed ID: 8666389
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  • 7. X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3.
    Zhu H, Shang D, Sun M, Choi S, Liu Q, Hao J, Figuera LE, Zhang F, Choy KW, Ao Y, Liu Y, Zhang XL, Yue F, Wang MR, Jin L, Patel PI, Jing T, Zhang X.
    Am J Hum Genet; 2011 Jun 10; 88(6):819-826. PubMed ID: 21636067
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  • 9. A new form of hypertrichosis inherited as an X-linked dominant trait.
    Macías-Flores MA, García-Cruz D, Rivera H, Escobar-Luján M, Melendrez-Vega A, Rivas-Campos D, Rodríguez-Collazo F, Moreno-Arellano I, Cantú JM.
    Hum Genet; 1984 Jun 10; 66(1):66-70. PubMed ID: 6698556
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  • 10. Congenital hypertrichosis universalis.
    Suskind R, Esterly NB.
    Birth Defects Orig Artic Ser; 1971 Jun 10; 7(8):103-6. PubMed ID: 5173252
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  • 14. Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation.
    Gedeon AK, Glass IA, Connor JM, Mulley JC.
    Am J Med Genet; 1996 Jul 12; 64(1):121-4. PubMed ID: 8826461
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  • 15. Linkage analysis of bipolar illness with X-chromosome DNA markers: a susceptibility gene in Xq27-q28 cannot be excluded.
    De bruyn A, Raeymaekers P, Mendelbaum K, Sandkuijl LA, Raes G, Delvenne V, Hirsch D, Staner L, Mendlewicz J, Van Broeckhoven C.
    Am J Med Genet; 1994 Dec 15; 54(4):411-9. PubMed ID: 7726217
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  • 18. Differentiation of congenital hypertrichosis from Ambras syndrome.
    Baumeister FA, Stengel-Rutkowski S.
    Clin Genet; 1994 Dec 15; 46(6):441. PubMed ID: 7889664
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  • 19. Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3.
    He PP, Zhang XJ, Yang Q, Li M, Liang YH, Yang S, Yan KL, Cui Y, Shen YY, Wang HY, Sun LD, Du WH, Shen YJ, Xu SJ, Huang W.
    Br J Dermatol; 2004 May 15; 150(5):837-42. PubMed ID: 15149494
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  • 20. A complex bilateral polysyndactyly disease locus maps to chromosome 7q36.
    Tsukurov O, Boehmer A, Flynn J, Nicolai JP, Hamel BC, Traill S, Zaleske D, Mankin HJ, Yeon H, Ho C.
    Nat Genet; 1994 Mar 15; 6(3):282-6. PubMed ID: 8012391
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