The FSH-inhibin axis in prader-willi syndrome: heterogeneity of gonadal dysfunction.
about
A case of familial central precocious puberty caused by a novel mutation in the makorin RING finger protein 3 gene.Prader-Willi Syndrome: A spectrum of anatomical and clinical features.Perspectives in Pediatric Pathology, Chapter 18. Hypogonadotropic Hypogonadisms. Pediatric and Pubertal Presentations.Review of Prader-Willi syndrome: the endocrine approach.Sexual dichotomy of gonadal function in Prader-Willi syndrome from early infancy through the fourth decade.
P2860
The FSH-inhibin axis in prader-willi syndrome: heterogeneity of gonadal dysfunction.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年學術文章
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2012年學術文章
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name
The FSH-inhibin axis in prader-willi syndrome: heterogeneity of gonadal dysfunction.
@ast
The FSH-inhibin axis in prader-willi syndrome: heterogeneity of gonadal dysfunction.
@en
type
label
The FSH-inhibin axis in prader-willi syndrome: heterogeneity of gonadal dysfunction.
@ast
The FSH-inhibin axis in prader-willi syndrome: heterogeneity of gonadal dysfunction.
@en
prefLabel
The FSH-inhibin axis in prader-willi syndrome: heterogeneity of gonadal dysfunction.
@ast
The FSH-inhibin axis in prader-willi syndrome: heterogeneity of gonadal dysfunction.
@en
P2093
P2860
P356
P1476
The FSH-inhibin axis in prader-willi syndrome: heterogeneity of gonadal dysfunction.
@en
P2093
Fortu Benarroch
Harry J Hirsch
Talia Eldar-Geva
Varda Gross-Tsur
P2860
P2888
P356
10.1186/1477-7827-10-39
P577
2012-05-06T00:00:00Z
P5875
P6179
1036425201