High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays

por Kothiyal, Prachi, Cox, Stephanie, Ebert, Jonathan, Husami, Ammar, Kenna, Margaret A, Greinwald, John H, Aronow, Bruce J, Rehm, Heidi L
Publicado 2010

A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness

por Bardien, Soraya, Human, Hannique, Harris, Tashneem, Hefke, Gwynneth, Veikondis, Rene, Schaaf, H Simon, van der Merwe, Lize, Greinwald, John H, Fagan, Johan, de Jong, Greetje
Publicado 2009