Ophthalmic Genetics,volume 20,issue 2  (06-2014)

Period of time: 2014年2期

Publisher: Informa Healthcare

Founded in: 1981

Total resources: 61

ISSN: 1381-6810

Subject: R77 Ophthalmology

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Ophthalmic Genetics,volume 20,issue 2

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Histopathology and molecular basis of iridogoniodysgenesis syndrome

By Pearce William G.,Mielke Bruce,Kulak Stephen C.,Walter Michael A. in (1999)

Ophthalmic Genetics,volume 20,issue 2 , Vol. 20, Iss. 2, 1999-06 , pp. 83-88

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EEM syndrome: report of a family and results of a ten-year follow-up

By Balarin Silva Valdir,Simões Andréa Mara,Marques-de-Faria Antonia Paula in (1999)

Ophthalmic Genetics,volume 20,issue 2 , Vol. 20, Iss. 2, 1999-06 , pp. 95-99

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Visual impairment and REP-1 gene mutations in Japanese choroideremia patients

By Hayakawa M.,Fujiki K.,Hotta Y.,Ito R.,Ohki J.,Ono J.,Saito A.,Nakayasu K.,Kanai A.,Ishidoh K.,Kominami E.,Yoshida K.,Kim K.C.,Ohashi H. in (1999)

Ophthalmic Genetics,volume 20,issue 2 , Vol. 20, Iss. 2, 1999-06 , pp. 107-115

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1147 del A mutation in the arrestin gene in Japanese patients with Oguchi disease

By Yamada Tetsuya,Matsumoto Masayuki,Kadoi Chiharu,Nagaki Yasunori,Hayasaka Yoriko,Hayasaka Seiji in (1999)

Ophthalmic Genetics,volume 20,issue 2 , Vol. 20, Iss. 2, 1999-06 , pp. 117-120

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Retinal degeneration associated with ectopia lentis

By Simonelli F.,De Crecchio G.,Testa F.,Nunziata G.,Mazzeo S.,Romano N.,Cavaliere L.,Rinaldi M.M.,Rinaldi E. in (1999)

Ophthalmic Genetics,volume 20,issue 2 , Vol. 20, Iss. 2, 1999-06 , pp. 121-126

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Retinitis pigmentosa, mental retardation, marked short stature, and brachydactyly in two sibs

By Lorda-Sanchez Isabel,Trujillo Maria Jose,Gimenez Ascensión,Garcia-Sandoval Blanca,Franco Angeles,Sanz Raul,Rodriguez de Alba Marta,Ramos Carmen,Ayuso Carmen in (1999)

Ophthalmic Genetics,volume 20,issue 2 , Vol. 20, Iss. 2, 1999-06 , pp. 127-131

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