[Monogenic and syndromic symptoms of morbid obesity. Rare but important].

about

[Monogenic and syndromic symptoms of morbid obesity. Rare but important].

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http://www.wikidata.org/entity/Q52870195

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh-hant

name

[Monogenic and syndromic symptoms of morbid obesity. Rare but important].

@en

[Monogenic and syndromic symptoms of morbid obesity. Rare but important].

@nl

type

Item

label

[Monogenic and syndromic symptoms of morbid obesity. Rare but important].

@en

[Monogenic and syndromic symptoms of morbid obesity. Rare but important].

@nl

prefLabel

[Monogenic and syndromic symptoms of morbid obesity. Rare but important].

@en

[Monogenic and syndromic symptoms of morbid obesity. Rare but important].

@nl

P1476

[Monogenic and syndromic symptoms of morbid obesity. Rare but important].

@en

P2093

H Krude

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

S Wiegand

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

P2860

Positional cloning of the mouse obese gene and its human homologue

Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene

Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans

20 years of leptin: human disorders of leptin action

Update on the genetics of bardet-biedl syndrome

Clinical spectrum of obesity and mutations in the melanocortin 4 receptor gene

Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity

Congenital leptin deficiency is associated with severe early-onset obesity in humans

Effects of recombinant leptin therapy in a child with congenital leptin deficiency.

Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

P304

111-2, 114-20

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P31

scholarly article

P356

10.1007/S00108-014-3532-8

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P407

Af-Jarmal

P433

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

P478

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

P577

2015-02-01T00:00:00Z

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P698

25630806

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