Period of time: 2014年2期
Publisher: Informa Healthcare
Founded in: 1981
Total resources: 61
ISSN: 1381-6810
Subject: R77 Ophthalmology
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Ophthalmic Genetics,volume 20,issue 2
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Dominant retinal dystrophies and Stargardt disease
Ophthalmic Genetics,volume 20,issue 2 , Vol. 20, Iss. 2, 1999-06 , pp.By Kniazeva Marina,Chiang Michael F.,Cutting Garry R.,Zack Donald J.,Han Min,Zhang Kang in (1999)
Ophthalmic Genetics,volume 20,issue 2 , Vol. 20, Iss. 2, 1999-06 , pp.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.No missense mutation in choroideremia patients analyzed to date
By Beaufrère Laurent,Claustres Mireille,Tuffery Sylvie in (1999)
Ophthalmic Genetics,volume 20,issue 2 , Vol. 20, Iss. 2, 1999-06 , pp.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.By Magli Adriano,De Marco Rocco,Capasso Luigi in (1999)
Ophthalmic Genetics,volume 20,issue 2 , Vol. 20, Iss. 2, 1999-06 , pp.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.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.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.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.