4 results for author:"Charlton R.S." in Literature citations
› Repeat search in UniProtKB (3)
|The common TMC1 mutation c.100C>T (p.Arg34X) is not a significant cause of deafness in British Asians.|
Searle C., Mavrogiannis L.A., Bennett C.P., Charlton R.S.
Genet Test Mol Biomarkers 16:453-455(2012) · Mapped (5)
|Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss.|
Yoong S.Y., Mavrogiannis L.A., Wright J., Fairley L., Bennett C.P., Charlton R.S., Spencer N.
Arch. Dis. Child. 96:798-803(2011) · Mapped (3)
|Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA.|
Taylor C.F., Charlton R.S., Burn J., Sheridan E., Taylor G.R.
|Investigations on a clinically and functionally unusual and novel germline p53 mutation.|
Rutherford J., Chu C.E., Duddy P.M., Charlton R.S., Chumas P., Taylor G.R., Lu X., Barnes D.M., Camplejohn R.S.