Simple and Efficient Identification of Rare Recessive Pathologically Important Sequence Variants from Next Generation Exome Sequence Data
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D. Bonthron | F. Alkuraya | A. Markham | C. Logan | I. Carr | S. Pena | Manir Ali | G. Black | J. Morgan | G. Taylor | C. Watson | S. Harrison | S. Melnik | C. Diggle | David T. Bonthron | Christine P. Diggle