Artigo Acesso aberto Revisado por pares

Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project

2009; Elsevier BV; Volume: 11; Issue: 12 Linguagem: Inglês

10.1097/gim.0b013e3181c371c5

ISSN

1530-0366

Autores

Richard G.H. Cotton, Aida I. Al Aqeel, Fahd Al‐Mulla, Paola Carrera, Mireille Claustres, Rosemary Ekong, V.J. Hyland, Finlay Macrae, Makia J. Marafie, Mark H. Paalman, George P. Patrinos, Ming Qi, Raj Ramesar, Rodney J. Scott, Rolf H. Sijmons, María-Jesús Sobrido, Mauno Vihinen,

Tópico(s)

Genetics, Bioinformatics, and Biomedical Research

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