Period of time: 2014年3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 31,issue 3
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eNOS gene polymorphism association with retinopathy in type 1 diabetes
By Bazzaz Javad Tavakkoly,Amoli Mahsa M.,Pravica Vera,Chandrasecaran Ramesh,Boulton Andrew J,Larijani Bagher,Hutchinson Ian V in (2010)
Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp.By Nikzamir Abdolrahim,Rashidi Armin,Esteghamati Alireza,Nakhjavani Manouchehr,Golmohammadi Taghi,Khalilzadeh Omid in (2010)
Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp.Long-term 12 year follow-up of X-linked congenital retinoschisis
By Kjellström Sten,Vijayasarathy Camasamudram,Ponjavic Vesna,Sieving Paul A.,Andréasson Sten in (2010)
Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp.Leber’s hereditary optic neuropathy: Clinical and molecular profile of a Brazilian sample
By Maciel-Guerra Andréa Trevas,Zanchetta Luciene Maria,Amaral Fernandes Marcela Scabello,Andrade Paula Baloni,do Amor Divino Miranda Paulo Maurício,Sartorato Edi Lúcia in (2010)
Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp.Mutation screen of β-crystallin genes in 274 patients with age-related macular degeneration
By Sturgill Gwen M.,Bala Elisa,Yaniglos Stacia S.,Peachey Neal S.,Hagstrom Stephanie A. in (2010)
Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp.By Curtin Jeremy,Moloney Greg,Grigg John,Sharota Franzco Dorian in (2010)
Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp.PITPNM3 is an uncommon cause of cone and cone-rod dystrophies
By Köhn Linda,Kohl Susanne,Bowne Sara J,Sullivan Lori S,Kellner Ulrich,Daiger Stephen P,Sandgren Ola,Golovleva Irina in (2010)
Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp.By Madhavan Jagadeesan,Mallikarjuna Kandalam,Vikas Khetan,George Ronnie,Bremner Rod,Kumaramanickavel Govindasamy in (2010)
Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp.Optic disk and white matter abnormalities in a patient with a
By Abu-Amero Khaled K.,Hellani Ali,Salih Mustafa A.,Alorainy Ibrahim A.,Zidan Ghassan,Kern Kyle C.,Sicotte Nancy L.,Bosley Thomas M. in (2010)
Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp.Familial case of Blau syndrome associated with a
By Villanueva-Mendoza Cristina,Arellanes-García Lourdes,Cubas-Lorenzo Victoria,Jimenez-Martinez Maria C.,Flores-Suárez Luis Felipe,Zenteno Juan Carlos in (2010)
Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp.