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Results 1 - 10 of 26 for ophthalmology
  1. Vitelliform macular dystrophy 
    ... best macular dystrophy associated with VMD2 gene mutations. Ophthalmology. 2005 Apr;112(4):586-92. doi: 10. ... age-related maculopathy, and bull's-eye maculopathy. Ophthalmology. 2001 Nov;108(11):2060-7. doi: 10. ...
    https://medlineplus.gov/.../condition/vitelliform-macular-dystrophy - Genetics
  2. Bradyopsia 
    ... vision): clinical features and course of the disease. Ophthalmology. 2007 Dec;114(12):2323-31. doi: 10. ... in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia). Ophthalmology. 2010 Jan;117(1):120-127.e1. doi: ...
    https://medlineplus.gov/genetics/condition/bradyopsia - Genetics
  3. Fundus albipunctatus 
    ... albipunctatus associated with compound heterozygous mutations in RPE65. Ophthalmology. 2011 May;118(5):888-94. doi: 10. ... AR. Phenotypic variability in RDH5 retinopathy (Fundus Albipunctatus). Ophthalmology. 2011 Aug;118(8):1661-70. doi: 10. ...
    https://medlineplus.gov/genetics/condition/fundus-albipunctatus - Genetics
  4. BEST1 gene 
    ... best macular dystrophy associated with VMD2 gene mutations. Ophthalmology. 2005 Apr;112(4):586-92. doi: 10. ... age-related maculopathy, and bull's-eye maculopathy. Ophthalmology. 2001 Nov;108(11):2060-7. doi: 10. ...
    https://medlineplus.gov/genetics/gene/best1 - Genetics
  5. RGS9BP gene 
    ... in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia). Ophthalmology. 2010 Jan;117(1):120-127.e1. doi: ...
    https://medlineplus.gov/genetics/gene/rgs9bp - Genetics
  6. ABCA4 gene 
    ... visual outcome in cone and cone-rod dystrophy. Ophthalmology. 2012 Apr;119(4):819-26. doi: 10. ...
    https://medlineplus.gov/genetics/gene/abca4 - Genetics
  7. CNGB3 gene 
    ... genes CNGA3 and CNGB3 in progressive cone dystrophy. Ophthalmology. 2010 Apr;117(4):825-30.e1. doi: ...
    https://medlineplus.gov/genetics/gene/cngb3 - Genetics
  8. X-linked infantile nystagmus 
    ... Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study. Ophthalmology. 2022 Jun;129(6):708-718. doi: 10. ...
    https://medlineplus.gov/.../condition/x-linked-infantile-nystagmus - Genetics
  9. CLRN1 gene 
    ... Hollander AI. CLRN1 mutations cause nonsyndromic retinitis pigmentosa. Ophthalmology. 2011 Jul;118(7):1444-8. doi: 10. ...
    https://medlineplus.gov/genetics/gene/clrn1 - Genetics
  10. MYO7A gene 
    ... Usher syndrome type 1 owing to MYO7A mutation. Ophthalmology. 2014 Feb;121(2):580-7. doi: 10. ...
    https://medlineplus.gov/genetics/gene/myo7a - Genetics
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