GENETIC SCREENING OF PATIENTS WITH CONGENITAL GH DEFICIENCY IN THE GENESIS OBSERVATIONAL PROGRAM: MUTATION FREQUENCY, PHENOTYPE AND GROWTH OUTCOMES

被引：0

作者：

Pfaeffle, Roland W. ^{[1
]}

Klammt, Juergen ^{[1
]}

Pfaeffle, Heike M. ^{[1
]}

Amselem, Serge ^{[2
]}

Legendre, Marie ^{[3
]}

Sobrier, Marie-Laure ^{[4
]}

Child, Christopher J. ^{[5
]}

Jones, Christine ^{[5
]}

Zimmermann, Alan G. ^{[5
]}

Blum, Werner F. ^{[6
]}

机构：

[1] Univ Leipzig, Leipzig, Germany

[2] Hop Enfants Armand Trousseau, Paris, France

[3] Hop Trousseau, Paris, France

[4] Inserm US013, Paris, France

[5] Eli Lilly & Co, Indianapolis, IN 46285 USA

[6] Univ Giessen, Giessen, Germany

来源：

HORMONE RESEARCH IN PAEDIATRICS | 2017年 / 88卷

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

FC2

引用

页码：3 / 4

页数：2

共 39 条

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