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  • JIMD Reports - Case and Research Reports, 2011/1

    Edición de SSIEM ...
    Series series Medicine (R0)
    JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. ... Leer más

    $89.99 USD

  • JIMD Reports - Case and Research Reports, 2012/1

    Edición de SSIEM ...
    Series series Medicine (R0)
    JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. ... Leer más

    $89.99 USD

  • JIMD Reports - Case and Research Reports, 2012/3

    Edición de SSIEM ...
    Series series Medicine (R0)
    JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. ... Leer más

    $89.99 USD

  • JIMD Reports - Case and Research Reports, 2012/2

    Edición de SSIEM ...
    Series series Biomedical and Life Sciences (R0)
    JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. ... Leer más

    $49.99 USD

  • JIMD Reports - Case and Research Reports, 2011/2

    Edición de SSIEM ...
    Series series Medicine (R0)
    JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. ... Leer más

    $89.99 USD

  • JIMD Reports - Case and Research Reports, 2011/3

    Edición de SSIEM ...
    Series series Medicine (R0)
    JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. ... Leer más

    $49.99 USD

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  • JIMD Reports, Volume 21

    Series series Medicine (R0)
    JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. ... Leer más

    $89.99 USD

  • JIMD Reports, Volume 17

    Series series Medicine (R0)
    JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. ... Leer más

    $49.99 USD

  • JIMD Reports - Case and Research Reports, 2012/5

    Series series Medicine (R0)
    JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. ... Leer más

    $89.99 USD

  • Laron Syndrome - From Man to Mouse

    Lessons from Clinical and Experimental Experience

    Edición de Zvi Laron, J. Kopchick ...
    Series series Medicine (R0)
    Laron syndrome (LS), or primary growth hormone (GH) insensitivity, was first described in 1966. Since then, many patients worldwide have been diagnosed with LS, which involves defects in the GH receptor that cause combined congenital deficiency of GH and IGF-I activities. In this comprehensive book the authors draw upon 50 years of multidisciplinary clinical and investigative follow-up of the ... Leer más

    $215.99 USD