The discovery of a Persian family with a form of Birt–Hogg–Dubé syndrome lacking the typical cutaneous stigmata of the syndrome-Reference-Cited by-同舟云学术

The discovery of a Persian family with a form of Birt–Hogg–Dubé syndrome lacking the typical cutaneous stigmata of the syndrome

Published:2013-01 Issue:1 Volume:37 Page:111-115
ISSN:0899-7071
Container-title:Clinical Imaging
language:en
Short-container-title:Clinical Imaging

Author:

Babaei Jandaghi Ali,Daliri Saeid,Kikkawa Mika,Khaledi Mojdeh,Soleimanifar Narjes,Alizadeh Ahmad,Habibzadeh Mahmoud,Haghi-Ashtiani Mohammad Taghi,Seyama Kuniaki,Rezaei Nima

Publisher

Elsevier BV

Subject

Radiology, Nuclear Medicine and imaging

Reference14 articles.

1. European BHD Consortium. Birt–Hogg–Dubé syndrome: diagnosis and management;Menko;Lancet Oncol,2009

2. BHD mutations, clinical and molecular genetic investigations of Birt–Hogg–Dubé syndrome: a new series of 50 families and a review of published reports;Toro;J Med Genet,2008

3. Mutations of the Birt Hogg Dubé gene in patients with multiple lung cysts and recurrent pneumothorax;Gunji;J Med Genet,2007

4. Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons;Birt;Arch Dermatol,1977

5. Birt–Hogg–Dubé syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2;Khoo;Oncogene,2001

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