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Journal Abstract Search

181 related items for PubMed ID: 1303285

  • 21. A novel aminoterminal mutation in the KAL-1 gene in a large pedigree with X-linked Kallmann syndrome.
    Gu WX, Colquhoun-Kerr JS, Kopp P, Bode HH, Jameson JL.
    Mol Genet Metab; 1998 Sep; 65(1):59-61. PubMed ID: 9787096
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  • 25. Unexpectedly similar rates of nucleotide substitution found in male and female hominids.
    Bohossian HB, Skaletsky H, Page DC.
    Nature; 2000 Aug 10; 406(6796):622-5. PubMed ID: 10949301
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  • 26. Accumulation of chloroplast DNA sequences on the Y chromosome of Silene latifolia.
    Kejnovsky E, Kubat Z, Hobza R, Lengerova M, Sato S, Tabata S, Fukui K, Matsunaga S, Vyskot B.
    Genetica; 2006 Aug 10; 128(1-3):167-75. PubMed ID: 17028949
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  • 27. Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome.
    Hardelin JP, Levilliers J, Blanchard S, Carel JC, Leutenegger M, Pinard-Bertelletto JP, Bouloux P, Petit C.
    Hum Mol Genet; 1993 Apr 10; 2(4):373-7. PubMed ID: 8504298
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  • 30. Reconstructing hominid Y evolution: X-homologous block, created by X-Y transposition, was disrupted by Yp inversion through LINE-LINE recombination.
    Schwartz A, Chan DC, Brown LG, Alagappan R, Pettay D, Disteche C, McGillivray B, de la Chapelle A, Page DC.
    Hum Mol Genet; 1998 Jan 10; 7(1):1-11. PubMed ID: 9384598
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  • 34. Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region.
    Meroni G, Franco B, Archidiacono N, Messali S, Andolfi G, Rocchi M, Ballabio A.
    Hum Mol Genet; 1996 Apr 10; 5(4):423-31. PubMed ID: 8845834
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  • 37. Frequent gene conversion events between the X and Y homologous chromosomal regions in primates.
    Iwase M, Satta Y, Hirai H, Hirai Y, Takahata N.
    BMC Evol Biol; 2010 Jul 23; 10():225. PubMed ID: 20650009
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