/
Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project
- Cotton, Richard G. H., Al Aqeel , Aida I., Patrinos, George P., Qi, Ming, Ramesar, Rajkumar S., Scott, Rodney J., Sijmons, Rolf H., Sobrido, Maria-Jesus, Vihinen, Mauno, Al-Mulla, Fahd, Carrera, Paola, Claustres, Mireille, Ekong, Rosemary, Hyland, Valentine J., Macrae, Finlay A., Marafie, Makia J., Paalman, Mark H.
Hereditary cancer in clinical practice transfers to BioMed Central (editorial)
- Lubiński, Jan, Sijmons, Rolf H., Scott, Rodney J.
Are you sure you would like to clear your session, including search history and login status?