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10篇 您的检索式:作者名="Norgett EE"
    题名 作者 年代 出处 被引量
1Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma显示文摘Norgett EE Hatsell SJ Carvajal-Huerta L 2000Hum Mol Genet2000,9,18:1
2Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy,woolly hair and keratoderma显示文摘Norgett EE Hatsell SJ Carvajal-Huerta L 2000Hum Mol Genet2000,9,18:1
3Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy,woolly hair and keratoderma显示文摘Norgett EE Hatsell S J Carvajal-Huerta L 2000Hum Mol Genet2000,9,:1
4Recessive muta- tion in desmoplakin disrupts desmoplakin-intermediate filament in- teractions and causes dilated cardiomyopathy, woolly hair and kera- toderma 显示文摘Norgett EE Hatsell SJ Carvajal-Huerta L 2000Hum Mol Genet2000,9,18:1
5Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma显示文摘Norgett EE Hatsell SJ Carvajal-Huerta L 2000Hum Mol Genet2000,9,18:1
6Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma 显示文摘Norgett EE Hatsell SJ Carvajal-Huerta L 2000Hum Mol Genet2000,9,18:1
7Recessive mutation in desmoplakin disrupts desmoplakin-intermediate fila- ment interactions and causes dilated cardiomyopathy, wolly hair and keratoderma显示文摘Norgett EE Hatsell SJ Carvajal-Huerta L 2000Hum Mol Genet2000,9,18:1
8Recessive mutation in desmoplakin disrupts desmoplakin-interme-diate filament interactions and causes dilated cardio-myopathy,woolly hair and keratoderma显示文摘 Hatsell SJ Carvajal-Huerta L 2000Hum MolGenet2000,9,18:1
9Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and eauses dilated eardiomyopathy,woolly hair and keratoderma显示文摘Norgett EE Hatsell SJ Carvajal-Huerta L 2000Hum Mol Genet2000,9,18:1
10Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis 显示文摘Kelsell DP Norgett EE Unsworth H 2005Am J Hum Genet2005,76,5:1
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