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Stone EM 3

Showing records 1 to 3 | Display all abstracts from Stone EM

18547 Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier
Craig JE; Baird PN; Healey DL; McNaught AI; McCartney PJ; Rait JL; Dickinson JL; Roe L; Fingert JH; Stone EM
Ophthalmology 2001; 108: 1607-1620

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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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18508 Delayed secondary glucocorticoid responsiveness of MYOC in human trabecular meshwork cells
Shepard AR; Jacobson N; Fingert JH; Stone EM; Sheffield VC; Clark AF
Investigative Ophthalmology and Visual Science 2001; 42: 3173-3181

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