All papers, people, and labs mentioned will appear here.
Ng, S.B. et al. Exome sequencing identifies the cause of a mendelian disorder. Nat. Genet. 42, 30-35 (2010). PMID 19915526
O'Roak, B.J. et al. Exome sequencing in soporadic autism spectrum disorders identifies severe de novo mutations. Nat. Genet. 43, 585-589 (2011). PMID 21572417
No comments:
Post a Comment