4
results
for author:"Stavrides G."
in Literature Citations
| Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy. Ayerdi-Izquierdo A., Stavrides G., Selles-Martinez J.J., Larrea L., Bovo G., Lopez de Munain A., Bisulli F., Marti-Masso J.F., Michelucci R., Poza J.J. et al. Epilepsy Res. 70:118-126(2006) · Mapped (2) |
| Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes. Silander K., Mohlke K.L., Scott L.J., Peck E.C., Hollstein P., Skol A.D., Jackson A.U., Deloukas P., Hunt S., Stavrides G. et al. Diabetes 53:1141-1149(2004) · Mapped (8) |
| The DNA sequence and comparative analysis of human chromosome 20. Deloukas P., Matthews L.H., Ashurst J.L., Burton J., Gilbert J.G.R., Jones M., Stavrides G., Almeida J.P., Babbage A.K., Bagguley C.L. et al. Nature 414:865-871(2001) · UniProtKB (802) |
| X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene. Knight S.W., Heiss N.S., Vulliamy T.J., Greschner S., Stavrides G., Pai G.S., Lestringant G., Varma N., Mason P.J., Dokal I. et al. Am. J. Hum. Genet. 65:50-58(1999) · UniProtKB (1) · Mapped (1) |
