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White, Stefan, Hewitt, Jacqueline, Turbitt, Erin, van der Zwan, Yvonne, Hersmus, Remko, Drop, Stenvert, Koopman, Peter, Harley, Vincent, Cools, Martine, Looijenga, Leendert and Sinclair. Andrew (2012) A multi-exon deletion within WWOX is associated with a 46,XY disorder of sex development. European Journal of Human Genetics, 20 3: 348-351. doi:10.1038/ejhg.2011.204 89   7 Cited 8 times in Scopus8 0
Fonseca, Dora Janeth, Ojeda, Diego, Lakhal, Besma, Braham, Rim, Eggers, Stefanie, Turbitt, Erin, White, Stefan, Landolsi, Hanene, Elghezal, Hatem, Saad, Ali, Restrepo, Carlos Martin, Fellous, Marc, Sinclair, Andrew, Koopman, Peter and Laissue, Paul (2012) CITED2 mutations potentially cause idiopathic premature ovarian failure. Translational Research, 160 5: 384-388. doi:10.1016/j.trsl.2012.05.006 72   2 Cited 2 times in Scopus2 0
White, Stefan, Ohnesorg, Thomas, Notini, Amanda, Roeszler, Kelly, Hewitt, Jacqueline, Daggag, Hinda, Smith, Craig, Turbitt, Erin, Gustin, Sonja, van den Bergen, Jocelyn, Miles, Denise, Western, Patrick, Arboleda, Valerie, Schumacher, Valerie, Gordon, Lavinia, Bell, Katrina, Bengtsson, Henrik, Speed, Terry, Hutson, John, Warne, Garry, Harley, Vincent, Koopman, Peter, Vilain, Eric and Sinclair, Andrew (2011) Copy number variation in patients with disorders of sex development due to 46,XY gonadal dysgenesis. PLoS One, 6 3: e17793.1-e17793.10. doi:10.1371/journal.pone.0017793 92   34 Cited 35 times in Scopus35 0