Sustained endocrine profiles of a girl with WAGR syndrome

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Sustained endocrine profiles of a girl with WAGR syndrome

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

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Sustained endocrine profiles of a girl with WAGR syndrome

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Sustained endocrine profiles of a girl with WAGR syndrome

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label

Sustained endocrine profiles of a girl with WAGR syndrome

@en

Sustained endocrine profiles of a girl with WAGR syndrome

@nl

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Sustained endocrine profiles of a girl with WAGR syndrome

@en

Sustained endocrine profiles of a girl with WAGR syndrome

@nl

P1476

Sustained endocrine profiles of a girl with WAGR syndrome

@en

P2093

Chad A Shaw

http://www.w3.org/2001/XMLSchema#string

Hiroyuki Torisu

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Kazuhiro Ohkubo

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Masafumi Sanefuji

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Michiko Torio

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Satoshi Akamine

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Shouichi Ohga

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Toshiro Hara

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Yoshito Ishizaki

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Yuhki Koga

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P2860

A de novo mutation affecting human TrkB associated with severe obesity and developmental delay

Brain-derived neurotrophic factor and obesity in the WAGR syndrome

Brain-derived neurotrophic factor regulates energy balance downstream of melanocortin-4 receptor

The BDNF val66met polymorphism affects activity-dependent secretion of BDNF and human memory and hippocampal function

Molecular and clinical studies in 138 Japanese patients with Silver-Russell syndrome

Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization.

Hyperphagia, severe obesity, impaired cognitive function, and hyperactivity associated with functional loss of one copy of the brain-derived neurotrophic factor (BDNF) gene.

Brain-derived neurotrophic factor-deficient mice develop aggressiveness and hyperphagia in conjunction with brain serotonergic abnormalities

Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism.

LGR4/GPR48 inactivation leads to aniridia-genitourinary anomalies-mental retardation syndrome defects.

P2888

s12881-017-0477-5

P304

117

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P31

scholarly article

case report

P356

10.1186/S12881-017-0477-5

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P433

http://www.w3.org/2001/XMLSchema#string

P478

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P50

Yasunari Sakai

M Kagami

P577

2017-10-23T00:00:00Z

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P6179

1092310886

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P698

29061165

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P932

5654094

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