Clinical features and an atypical WT1 mutant site in a child with incomplete Denys-Drash syndrome.

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Clinical features and an atypical WT1 mutant site in a child with incomplete Denys-Drash syndrome.

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2014 nî lūn-bûn

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2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

2014年论文

@zh

2014年论文

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Clinical features and an atypi ...... complete Denys-Drash syndrome.

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Clinical features and an atypi ...... complete Denys-Drash syndrome.

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Clinical features and an atypi ...... complete Denys-Drash syndrome.

@en

Clinical features and an atypi ...... complete Denys-Drash syndrome.

@nl

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Clinical features and an atypi ...... complete Denys-Drash syndrome.

@en

Clinical features and an atypi ...... complete Denys-Drash syndrome.

@nl

P1476

Clinical features and an atypi ...... complete Denys-Drash syndrome.

@en

P2093

Hai-Yan Wang

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Jia-Cong Mo

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Jun-Jie Sun

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Liang-Zhong Sun

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Ying Mo

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Zhi-Hui Yue

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P2860

A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46,XY patient with Denys-Drash syndrome

Coronary vessel development requires activation of the TrkB neurotrophin receptor by the Wilms' tumor transcription factor Wt1.

Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database

An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis.

The podocyte as a target: cyclosporin A in the management of the nephrotic syndrome caused by WT1 mutations.

Case report: WT1 exon 6 truncation mutation and ambiguous genitalia in a patient with Denys-Drash syndrome.

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647-649

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scholarly article

P356

10.4103/1008-682X.125396

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P433

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P478

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P577

2014-07-01T00:00:00Z

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P698

24625882

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P932

4104105

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