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	题名	作者	年代	出处	被引量
1	Confirmation of the 14568 mutation in the mitochondrial ND6 gene as causative in Leber's hereditary optic neumpathy 显示文摘	Fauser S Leo-Kottler B Beseh D	2002	Ophthalmic Genet2002，23，3：	1
2	Electroretinographic findings in Duchenne/Becker muscular dystrophy and correlation with genotype显示文摘	Ulgenalp A Oner FH Soylev MF	2002	Ophthalmic Genet2002，23，3：	1
3	Differentiating Alstr?m from Bardet-Biedl syndrome (BBS) using systematic ciliopathy genes sequencing显示文摘	K. Aliferis S. Hellé G. Gyapay S. Duchatelet C. Stoetzel J.-L. Mandel H. Dollfus	2012	Ophthalmic Genetics2012，，1：	1
4	A discordant sib-pair linkage analysis of age-related macular degeneration显示文摘	SL Santangelo C H Yen S Haddad	2005	Ophthalmic Genet2005，26，：	1
5	Congenital nasolacrimal duct occlusion with clinical anophthalmos:a possible new as- sociation显示文摘	Oguz H Ozturk A San I	2003	Ophthalmic Genet2003，24，3：	1
6	Familial case of Blau syndrome associated with a CARDI5/ NOD2 mutation显示文摘	Villanueva-Mendoza C Arellanes-Garcia L Cubas-Lorenzo V	2010	Ophthalmic Genet2010，31，3：	1
7	Association of VEGF gene polymorphisms with diabetic retinopathy in a south Indian cohort显示文摘	Uthra S Raman R Mukesh BN	2008	Ophthalmic Genet2008，29，1：	1
8	Nitric oxide synthase 3(NOS3)4b/a,T-786C and G894T polymorphisms in association with diabetic retinopathy susceptibility:a meta-analysis显示文摘	Zhao S Li T Zheng B	2012	Ophthalmic Genet2012，33，4：	1
9	Preferential looking-clinical lessons显示文摘	Fielder AR DobsonV Moseley MJ	1992	Ophthalmic Pasdiatr Genet1992，13，2：	1
10	The relationship between ACE gene insertionideletion polymorphism and diabetic retinopathy in I- ranian patients with type 2 diabetes 显示文摘	Nikzamir A Rashidi A Esteghamati A Nakbjavani M Golmo- hammadi T Khalilzadeh O	2010	Ophthalmic Genet2010，31，3：	1
11	Further refinement of the MYP2locus for autosomal dominant high myopia by linkage disequilibrium analysis显示文摘	Yong TL Atwood LD Ronan SM	2001	Ophthalmic Genet2001，22，：	1
12	A point mutation in the RDS-peripherin gene in a Spanish family with central areolar choroidal dystrophy显示文摘	Serra A Gean E	1995	Ophthalmic Genet1995，16，2：	1
13	A Novel NDP Mutation in anInfant with Unilateral Persistent Fetal Vasculature and Retinal Vascu-lopathy 显示文摘	Aponte EP Pulido JS Ellison JW	2009	Ophthalmic Genet2009，30，2：	1
14	The association of age-related maculopathy susceptibility 2(ARMS2)and complement factor H(CFH)variants with two angiographic subtypes of polypoidal choroidal vaseulopathy显示文摘	Miki A Honda S Kondo N	2013	Ophthalmic Genet2013，34，：	1
15	Exfoliation syndrome:clinical and genetic features显示文摘	Orr AC Robitaille JM Price PA	2001	Ophthalmic Genet2001，22，：	1
16	A review of the molecular genetics of congenital Idiopathic Nystagmus ( CIN )显示文摘	Self J Lotery A	2007	Ophthalmic Genet2007，28，4：	1
17	Ophthalmic Genetics in China显示文摘	Dan-Ning Hu	1983	Ophthalmic Genetics1983，，1：	1
18	Ocular manifestations of the autoinflammatory syndromes 显示文摘	Tarabishy AB Hise AG Traboulsi El	2012	Ophthalmic Genet2012，33，4：	1
19	A Novel NDP Mutation in an Infant with Unilateral Persistent Fetal Vasculature and Retinal Vasculopathy显示文摘	Elisabeth P. Aponte Jose S. Pulido Jay W. Ellison Polly A. Quiram Brian G. Mohney	2009	Ophthalmic Genetics2009，，2：	1
20	Combined occurrence of autosomal dominant aniridia and autosomal recessive albinism in several members of a family 显示文摘	YAHALOM C SHARON D DALIA E SIMHON SB SHEMESH E BLUMENFELD A	2015	Ophthalmic Genet2015，36，2：	1

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