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
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D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
FC2
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收藏
页码：3 / 4
页数：2
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