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Journal Abstract Search

177 related items for PubMed ID: 8504298

  • 1. 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; 2(4):373-7. PubMed ID: 8504298
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  • 2. The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics.
    Oliveira LM, Seminara SB, Beranova M, Hayes FJ, Valkenburgh SB, Schipani E, Costa EM, Latronico AC, Crowley WF, Vallejo M.
    J Clin Endocrinol Metab; 2001 Apr; 86(4):1532-8. PubMed ID: 11297579
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  • 9. Molecular analysis of KAL-1, GnRH-R, NELF and EBF2 genes in a series of Kallmann syndrome and normosmic hypogonadotropic hypogonadism patients.
    Trarbach EB, Baptista MT, Garmes HM, Hackel C.
    J Endocrinol; 2005 Dec; 187(3):361-8. PubMed ID: 16423815
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  • 11. A novel nonsense mutation of the KAL gene in two brothers with Kallmann syndrome.
    Jansen C, Hendriks-Stegeman BI, Jansen M.
    Horm Res; 2000 Dec; 53(4):207-12. PubMed ID: 11044805
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  • 13. Analysis of the KAL1 gene in 19 Japanese patients with Kallmann syndrome.
    Izumi Y, Tatsumi K, Okamoto S, Ogawa T, Hosokawa A, Matsuo T, Kato Y, Fukui H, Amino N.
    Endocr J; 2001 Apr; 48(2):143-9. PubMed ID: 11456260
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  • 14. Kallmann syndrome gene (KAL-X) is not mutated in schizophrenia.
    O'Neill M, Brewer W, Thornley C, Copolov D, Warne G, Sinclair A, Forrest S, Williamson R.
    Am J Med Genet; 1999 Feb 05; 88(1):34-7. PubMed ID: 10050964
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