advertisement

---

Kehl HG 1

Showing records 1 to 1 | Display all abstracts from Kehl HG

52930 Singleton-Merten syndrome: an autosomal dominant disorder with variable expression
Feigenbaum A; Müller C; Yale C; Kleinheinz J; Jezewski P; Kehl HG; MacDougall M; Rutsch F; Hennekam RC
American Journal of Medical Genetics, Part A 2013; 161: 360-370

---