First Case Report of Prader-Willi-Like Syndrome in Colombia.

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First Case Report of Prader-Willi-Like Syndrome in Colombia.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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First Case Report of Prader-Willi-Like Syndrome in Colombia.

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First Case Report of Prader-Willi-Like Syndrome in Colombia.

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label

First Case Report of Prader-Willi-Like Syndrome in Colombia.

@en

First Case Report of Prader-Willi-Like Syndrome in Colombia.

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First Case Report of Prader-Willi-Like Syndrome in Colombia.

@en

First Case Report of Prader-Willi-Like Syndrome in Colombia.

@nl

P1476

First Case Report of Prader-Willi-Like Syndrome in Colombia.

@en

P2093

Estephania Candelo

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Harry Pachajoa

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Juan F Gomez

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P2860

Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype

Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome

Profound obesity associated with a balanced translocation that disrupts the SIM1 gene.

Prader-Willi-like phenotypes: a systematic review of their chromosomal abnormalities.

Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1.

Rare variants in single-minded 1 (SIM1) are associated with severe obesity.

Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features

De novo interstitial deletion q16.2q21 on chromosome 6.

Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?

Interstitial deletions of chromosome 6q: genotype-phenotype correlation utilizing array CGH.

P304

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scholarly article

case report

P356

10.3389/FGENE.2018.00098

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P478

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P50

Max M Feinstein

Diana Ramírez-Montaño

P577

2018-03-21T00:00:00Z

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P698

29619043

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P932

5871659

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