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Article

A BHD germline mutation identified in an Asian family with Birt-Hogg-Dubé syndrome.

Acta dermato-venereologica - 1 Jan 2008

Misago Noriyuki, Joh Keiichiro, Yatsuki Hitomi, Soejima Hidenobu, Narisawa Yutaka

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PMID: 18709329
DOI: 10.2340/00015555-0439

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A BHD germline mutation identified in an Asian family with Birt-Hogg-Dubé syndrome.PMID 18709329Read ↗

Molecular genetics and clinical features of Birt–Hogg–Dubé syndromeSemantic proximity Read ↗

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High Frequency of Somatic Frameshift BHD Gene Mutations in Birt-Hogg-Dubé–Associated Renal TumorsSemantic proximity Read ↗

Birt-Hogg-Dubé syndrome in an African patient and a novel mutation in the FLCN gene.Semantic proximity Read ↗

Case Report of Birt–Hogg–Dubé SyndromeSemantic proximity Read ↗

Birt-Hogg-Dubé syndrome with novel FLCN gene mutations and different clinical presentations: Case series.Semantic proximity Read ↗

Genetic Insight into Birt-Hogg-Dubé syndrome in Indian patients reveals novel mutations in <i>FLCN</i>Semantic proximity Read ↗

Genetic insight into Birt-Hogg-Dubé syndrome in Indian patients reveals novel mutations at FLCN.Semantic proximity Read ↗

Birt-Hogg-Dubé Syndrome: Clinical and Genetic Studies of 20 FamiliesSemantic proximity Read ↗

Identification and characterization of Birt-Hogg-Dubé associated renal carcinoma.Semantic proximity Read ↗

Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dubé syndrome.Semantic proximity Read ↗

Birt-Hogg-Dubé syndrome: diagnosis and managementSemantic proximity Read ↗

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