Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome)

Citation:

Hoffer JL, Fryssira H, Konstantinidou AE, Ropers HH, Tzschach A. Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome). Clinical genetics. 2013;83(1):92-95.