Browsing Centre for Genomics and Child Health by Author "Futreal, PA"
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Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma
Varela, I; Tarpey, P; Raine, K; Huang, D; Ong, CK; Stephens, P; Davies, H; Jones, D; Lin, ML; Teague, J (2011-01-27) -
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus
Tarpey, P; Thomas, S; Sarvananthan, N; Mallya, U; Lisgo, S; Talbot, CJ; Roberts, EO; Awan, M; Surendran, M; McLean, RJ (2006-11)