Search Results - Permutt, M.Alan

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  1. 1
    Identification of a Human LMX1 (LMX1.1)-Related Gene, LMX1.2: Tissue-Specific Expression and Linkage Mapping on Chromosome 9

    Identification of a Human LMX1 (LMX1.1)-Related Gene, LMX1.2: Tissue-Specific Expression and Linkage Mapping on Chromosome 9 by Iannotti, Christopher A., Inoue, Hiroshi, Bernal, Ernesto, Aoki, Minoru, Liu, Li, Donis-Keller, Helen, German, Michael S., Permutt, M.Alan

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  2. 2
    Isolation, Characterization, and Chromosomal Mapping of the Human Nkx6.1 Gene (NKX6A), a New Pancreatic Islet Homeobox Gene

    Isolation, Characterization, and Chromosomal Mapping of the Human Nkx6.1 Gene (NKX6A), a New Pancreatic Islet Homeobox Gene by Inoue, Hiroshi, Rudnick, Abraham, German, Michael S., Veile, Rosalie, Donis-Keller, Helen, Permutt, M.Alan

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  3. 3
    Searching for Type 2 Diabetes Genes in the Post-genome Era

    Searching for Type 2 Diabetes Genes in the Post-genome Era by Permutt, M.Alan, Hattersley, Andrew T.

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  4. 4
    Familial hyperinsulinism with apparent autosomal dominant inheritance: Clinical and genetic differences from the autosomal recessive variant

    Familial hyperinsulinism with apparent autosomal dominant inheritance: Clinical and genetic differences from the autosomal recessive variant by Thornton, Paul S., Satin-Smith, Marta S., Herold, Kevan, Glaser, Benjamin, Chiu, Ken C., Nestorowicz, Ann, Permutt, M.Alan, Baker, Lester, Stanley, Charles A.

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  5. 5
    Neonatal Hyperinsulinism

    Neonatal Hyperinsulinism by Glaser, Benjamin, Landau, Heddy, Permutt, M.Alan

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  6. 6
    Human Cholecystokinin Type A Receptor Gene: Cytogenetic Localization, Physical Mapping, and Identification of Two Missense Variants in Patients with Obesity and Non-Insulin-Dependent Diabetes Mellitus (NIDDM)

    Human Cholecystokinin Type A Receptor Gene: Cytogenetic Localization, Physical Mapping, and Identification of Two Missense Variants in Patients with Obesity and Non-Insulin-Depende... by Inoue, Hiroshi, Iannotti, Christopher A., Welling, Cris M., Veile, Rosalie, Donis-Keller, Helen, Permutt, M.Alan

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  7. 7
    Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews

    Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews by Glaser, Benjamin, Chiu, Ken C., Liu, Li, Anker, Roberto, Nestorowicz, Ann, Cox, Nancy J., Landau, Heddy, Nurit, Kalser, Thornton, Paul S., Stanley, Charles A., Cerasl, Erol, Baker, Lester, Donis-Keller, Helen, Permutt, M.Alan

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  8. 8
    Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews

    Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews by Glaser, Benjamin, Chiu, Ken C., Liu, Li, Anker, Roberto, Nestorowicz, Ann, Cox, Nancy J., Landau, Heddy, Kaiser, Nurit, Thornton, Paul S., Stanley, Charles A., Cerasi, Erol, Baker, Lester, Donis-Keller, Helen, Permutt, M.Alan

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