au.\*:("CARRIERO, Nicholas J")
Results 1 to 3 of 3
Selection :
De novo mutations revealed by whole-exome sequencing are strongly associated with autismSANDERS, Stephan J; MURTHA, Michael T; WALKER, Michael F et al.Nature (London). 2012, Vol 485, Num 7397, pp 237-241, issn 0028-0836, 5 p.Article
Ultrasensitive Measurement of Hotspot Mutations in Tumor DNA in Blood Using Error-Suppressed Multiplexed Deep SequencingNARAYAN, Azeet; CARRIERO, Nicholas J; GETTINGER, Scott N et al.Cancer research (Chicago, Ill.). 2012, Vol 72, Num 14, pp 3492-3498, issn 0008-5472, 7 p.Article
Paired-end mapping reveals extensive structural variation in the human genomeKORBEL, Jan O; ECKEHART URBAN, Alexander; TAILLON, Bruce E et al.Science (Washington, D.C.). 2007, Vol 318, Num 5849, pp 420-426, issn 0036-8075, 7 p.Article