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BIGH3 mutation spectrum in corneal dystrophies.
Munier FL, Frueh BE, Othenin-Girard P, Uffer S, Cousin P, Wang MX, Héon E, Black GC, Blasi MA, Balestrazzi E, Lorenz B, Escoto R, Barraquer R, Hoeltzenbein M, Gloor B, Fossarello M, Singh AD, Arsenijevic Y, Zografos L, Schorderet DF. Munier FL, et al. Among authors: wang mx. Invest Ophthalmol Vis Sci. 2002 Apr;43(4):949-54. Invest Ophthalmol Vis Sci. 2002. PMID: 11923233
Mutation hot spots in 5q31-linked corneal dystrophies.
Korvatska E, Munier FL, Djemaï A, Wang MX, Frueh B, Chiou AG, Uffer S, Ballestrazzi E, Braunstein RE, Forster RK, Culbertson WW, Boman H, Zografos L, Schorderet DF. Korvatska E, et al. Among authors: wang mx. Am J Hum Genet. 1998 Feb;62(2):320-4. doi: 10.1086/301720. Am J Hum Genet. 1998. PMID: 9463327 Free PMC article.
Molecular genetics of retinoblastoma.
Zhang K, Wang MX, Munier F, Roth D, Mastrangelo D, Chung S, Shields JA, Donoso LA. Zhang K, et al. Among authors: wang mx. Int Ophthalmol Clin. 1993 Summer;33(3):53-65. doi: 10.1097/00004397-199303330-00010. Int Ophthalmol Clin. 1993. PMID: 8104909 Review. No abstract available.
Genetic aspects of uveal melanoma: a brief review.
Singh AD, Wang MX, Donoso LA, Shields CL, De Potter P, Shields JA. Singh AD, et al. Among authors: wang mx. Semin Oncol. 1996 Dec;23(6):768-72. Semin Oncol. 1996. PMID: 8970601 Review.
828 results