Congenital Hypogonadotropic Hypogonadism during Childhood: Presentation and Genetic Analyses in 46 Boys
出版年份 2013 全文链接
标题
Congenital Hypogonadotropic Hypogonadism during Childhood: Presentation and Genetic Analyses in 46 Boys
作者
关键词
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出版物
PLoS One
Volume 8, Issue 10, Pages e77827
出版商
Public Library of Science (PLoS)
发表日期
2013-10-25
DOI
10.1371/journal.pone.0077827
参考文献
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- The Results ofCHD7Analysis in Clinically Well-Characterized Patients with Kallmann Syndrome
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- Approach to the Male Patient with Congenital Hypogonadotropic Hypogonadism
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- Longitudinal Evaluation of the Hypothalamic-Pituitary-Testicular Function in 8 Boys with Adrenal Hypoplasia Congenita (AHC) Due to NR0B1 Mutations
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- (2009) Julie Sarfati et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- GNRH1mutations in patients with idiopathic hypogonadotropic hypogonadism
- (2009) Yee-Ming Chan et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
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- TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction
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