Clinical and molecular characteristics in 15 patients with androgen receptor gene mutations from South China.

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Clinical and molecular characteristics in 15 patients with androgen receptor gene mutations from South China.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

@yue

2017年論文

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2017年論文

@zh-hk

2017年論文

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2017年論文

@zh-tw

2017年论文

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2017年论文

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2017年论文

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Clinical and molecular charact ...... ne mutations from South China.

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Clinical and molecular charact ...... ne mutations from South China.

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Clinical and molecular charact ...... ne mutations from South China.

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P1476

Clinical and molecular charact ...... ne mutations from South China.

@en

P2093

G Liu

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H Sheng

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J Cheng

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L Liu

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L Su

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Q Shi

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X Yin

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Y Cai

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Z Lu

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P2860

Oligospermic infertility associated with an androgen receptor mutation that disrupts interdomain and coactivator (TIF2) interactions

Male infertility and androgen receptor gene mutations: clinical features and identification of seven novel mutations

Isolated micropenis reveals partial androgen insensitivity syndrome confirmed by molecular analysis

Promoter-dependent activity on androgen receptor N-terminal domain mutations in androgen insensitivity syndrome.

Novel (60%) and recurrent (40%) androgen receptor gene mutations in a series of 59 patients with a 46,XY disorder of sex development.

Androgen insensitivity syndrome.

Mutations in the ligand-binding domain of the androgen receptor gene cluster in two regions of the gene.

Mutation of the androgen receptor (R840S) in an Egyptian patient with partial androgen insensitivity syndrome: review of the literature on the clinical expression of different R840 substitutions.

The Wilms tumor suppressor WT1 regulates early gonad development by activation of Sf1.

A Recurrent Germline Mutation in the 5'UTR of the Androgen Receptor Causes Complete Androgen Insensitivity by Activating Aberrant uORF Translation.

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scholarly article

P356

10.1111/AND.12763

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P577

2017-03-06T00:00:00Z

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P698

28261839

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