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Page 1
Ophthalmic features of CHARGE syndrome with CHD7 mutations.
Nishina S, Kosaki R, Yagihashi T, Azuma N, Okamoto N, Hatsukawa Y, Kurosawa K, Yamane T, Mizuno S, Tsuzuki K, Kosaki K. Nishina S, et al. Am J Med Genet A. 2012 Mar;158A(3):514-8. doi: 10.1002/ajmg.a.34400. Epub 2012 Feb 2. Am J Med Genet A. 2012. PMID: 22302456
PAX6 missense mutation in isolated foveal hypoplasia.
Azuma N, Nishina S, Yanagisawa H, Okuyama T, Yamada M. Azuma N, et al. Among authors: nishina s. Nat Genet. 1996 Jun;13(2):141-2. doi: 10.1038/ng0696-141. Nat Genet. 1996. PMID: 8640214 No abstract available.
CD44 expression in the developing human retina.
Nishina S, Hirakata A, Hida T, Sawa H, Azuma N. Nishina S, et al. Graefes Arch Clin Exp Ophthalmol. 1997 Feb;235(2):92-6. doi: 10.1007/BF00941736. Graefes Arch Clin Exp Ophthalmol. 1997. PMID: 9147957
PAX6 expression in the developing human eye.
Nishina S, Kohsaka S, Yamaguchi Y, Handa H, Kawakami A, Fujisawa H, Azuma N. Nishina S, et al. Br J Ophthalmol. 1999 Jun;83(6):723-7. doi: 10.1136/bjo.83.6.723. Br J Ophthalmol. 1999. PMID: 10340984 Free PMC article.
230 results