Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project.
Cotton RG, Al Aqeel AI, Al-Mulla F, Carrera P, Claustres M, Ekong R, Hyland VJ, Macrae FA, Marafie MJ, Paalman MH, Patrinos GP, Qi M, Ramesar RS, Scott RJ, Sijmons RH, Sobrido MJ, Vihinen M; members of the Human Variome Project Data Collection from Clinics, Data Collection from Laboratories and Publication, Credit and Incentives Working Groups.
Cotton RG, et al. Among authors: patrinos gp.
Genet Med. 2009 Dec;11(12):843-9. doi: 10.1097/GIM.0b013e3181c371c5.
Genet Med. 2009.
PMID: 20010362
Free article.