advertisement

---

Alward WLM 2

Showing records 1 to 2 | Display all abstracts from Alward WLM

8667 A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene
Honkanen RA; Nishimura DY; Swiderski RE; Bennett SR; Hong S; Kwon YH; Stone EM; Sheffield VC; Alward WLM
American Journal of Ophthalmology 2003; 135: 368-375

---

8600 Gonioscopy in primary angle closure glaucoma
Bruno CA; Alward WLM
Seminars in Ophthalmology 2002; 17: 59-68

---