Clinical and genetic study of a large Chinese family presented with familial spontaneous pneumothorax.

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Clinical and genetic study of a large Chinese family presented with familial spontaneous pneumothorax.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

Clinical and genetic study of ...... lial spontaneous pneumothorax.

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label

Clinical and genetic study of ...... lial spontaneous pneumothorax.

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prefLabel

Clinical and genetic study of ...... lial spontaneous pneumothorax.

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P1476

Clinical and genetic study of ...... lial spontaneous pneumothorax.

@en

P2093

Fan Yang

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Guanchao Jiang

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Huajie Xing

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Jun Wang

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Xiao Li

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Yanguo Liu

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Yanyan Hou

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P2860

BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dubé syndrome: a new series of 50 families and a review of published reports

Folliculin controls lung alveolar enlargement and epithelial cell survival through E-cadherin, LKB1, and AMPK.

A 4-bp deletion in the Birt-Hogg-Dubé gene (FLCN) causes dominantly inherited spontaneous pneumothorax.

Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dubé syndrome

Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2.

Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons.

Clinical and genetic spectrum of Birt-Hogg-Dube syndrome patients in whom pneumothorax and/or multiple lung cysts are the presenting feature

Familial spontaneous pneumothorax.

Birt-Hogg-Dubé syndrome: diagnosis and management.

Clinical and genetic studies of Birt-Hogg-Dubé syndrome.

P304

1967-1972

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scholarly article

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10.21037/JTD.2017.06.69

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P433

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P478

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P577

2017-07-01T00:00:00Z

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P698

28839995

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P921

pneumothorax

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5542951

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