Resultados de procura - Rhead, William J.

Novel B3GALTL mutations in classic Peters Plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes por Weh, Eric, Reis, Linda M., Tyler, Rebecca C., Bick, David, Rhead, William J., Wallace, Stephanie, McGregor, Tracy L., Dills, Shelley K., Chao, Mei-Chyn, Murray, Jeffrey C., Semina, Elena V.

Ligazón do recurso Ligazón do recurso Ligazón do recurso

Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation por Kurtz, David M., Rinaldo, Piero, Rhead, William J., Tian, Liqun, Millington, David S., Vockley, Jerry, Hamm, Doug A., Brix, Amy E., Lindsey, J. Russell, Pinkert, Carl A., O’Brien, William E., Wood, Philip A.

Ligazón do recurso Ligazón do recurso

Mutations in KAT6B, Encoding a Histone Acetyltransferase, Cause Genitopatellar Syndrome por Campeau, Philippe M., Kim, Jaeseung C., Lu, James T., Schwartzentruber, Jeremy A., Abdul-Rahman, Omar A., Schlaubitz, Silke, Murdock, David M., Jiang, Ming-Ming, Lammer, Edward J., Enns, Gregory M., Rhead, William J., Rowland, Jon, Robertson, Stephen P., Cormier-Daire, Valérie, Bainbridge, Matthew N., Yang, Xiang-Jiao, Gingras, Marie-Claude, Gibbs, Richard A., Rosenblatt, David S., Majewski, Jacek, Lee, Brendan H.

Ligazón do recurso Ligazón do recurso Ligazón do recurso