4 results for author:"Charlton R.S." in Literature citations
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| 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. Br. J. Cancer 86:1592-1596(2002) · UniProtKB (1) · Mapped (31) |