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Kawase C 1

Showing records 1 to 1 | Display all abstracts from Kawase C

18543 Screening for mutations of Axenfeld-Rieger syndrome caused by FOXC1 gene in Japanese patients
Kawase C; Kawase K; Taniguchi T; Sugiyama K; Yamamoto T; Kitazawa Y; Alward WL; Stone EM; Nishimura DY; Sheffield VC
Journal of Glaucoma 2001; 10: 477-482

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