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Venturini C 2
Showing records 1 to 2 | Display all abstracts from Venturini C58892 Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness
Davidson AE; Cheong SS; Hysi PG; Venturini C; Plagnol V; Ruddle JB; Ali H; Carnt N; Gardner JC; Hassan H; Gade E; Kearns L; Jelsig AM; Restori M; Webb TR; Laws D; Cosgrove M; Hertz JM; Russell-Eggitt I; Pilz DT; Hammond CJ; Tuft SJ; Hardcastle AJ
PLoS ONE 2014; 9: e104163
59028 Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
Hysi PG; Cheng CY; Springelkamp H; Macgregor S; Bailey JN; Wojciechowski R; Vitart V; Nag A; Hewitt AW; Höhn R; Venturini C; Mirshahi A; Ramdas WD; Thorleifsson G; Vithana E; Khor CC; Stefansson AB; Liao J; Haines JL; Amin N; Wang YX; Wild PS; Ozel A
Nature Genetics 2014; 46: 1126-1130