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BHD mutations, clinical and molecular genetic investigations of Birt–Hogg–Dubé syndrome: a new series of 50 families and a review of published reports
- Dr J R Toro, Genetic Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, 6120 Executive Boulevard, Executive Plaza South, Room 7012, Rockville, MD 20892-7231, USA; torojo{at}mail.nih.gov
Citation
BHD mutations, clinical and molecular genetic investigations of Birt–Hogg–Dubé syndrome: a new series of 50 families and a review of published reports
Publication history
- Received September 6, 2007
- Revised December 20, 2007
- Accepted December 21, 2007
- First published January 30, 2008.
Online issue publication
July 29, 2016
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- Previous version (27 April 2016).
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2008 BMJ Publishing Group Ltd