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Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations
- Correspondence to: Dr J Berg, Department of Medical & Molecular Genetics, GKT School of Medicine, King’s College London, 8th Floor Guy’s Tower, Guy’s Hospital, London SE1 9RT, UK; jonathan.berg{at}kcl.ac.uk
Citation
Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations
Publication history
- Accepted May 9, 2003
- Revised May 9, 2003
- First published August 14, 2003.
Online issue publication
August 14, 2003
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Copyright 2003 Journal of Medical Genetics