生长激素缺乏症相关的复杂疾病表型与生长激素-1基因的一种新型异常缺陷有关。 - Suppr

Complex disease phenotype revealed by GH deficiency associated with a novel and unusual defect in the GH-1 gene.

作者信息

Iughetti Lorenzo, Sobrier Marie-Laure, Predieri Barbara, Netchine Irene, Carani Cesare, Bernasconi Sergio, Balli Fiorella, Amselem Serge

出版信息

Clin Endocrinol (Oxf). 2008 Jul;69(1):170-2. doi: 10.1111/j.1365-2265.2007.03157.x. Epub 2008 Jul 1.

DOI:10.1111/j.1365-2265.2007.03157.x

PMID:18088397

Abstract

摘要

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Complex disease phenotype revealed by GH deficiency associated with a novel and unusual defect in the GH-1 gene.生长激素缺乏症相关的复杂疾病表型与生长激素-1基因的一种新型异常缺陷有关。

Clin Endocrinol (Oxf). 2008 Jul;69(1):170-2. doi: 10.1111/j.1365-2265.2007.03157.x. Epub 2008 Jul 1.

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Growth hormone deficiency: transition from adolescence to adulthood. Highlights from a Latin-American Serono Symposia International Foundation Conference.生长激素缺乏症：从青少年到成年的转变。拉丁美洲赛诺菲国际基金会会议亮点

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Pituitary gene mutations and the growth hormone pathway.垂体基因突变与生长激素通路

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Complex disease phenotype revealed by GH deficiency associated with a novel and unusual defect in the GH-1 gene.

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