Letter: Autosomal dominant inheritance in albinism

A G1103R mutation in CRB1 is co-inherited with high hyperopia and Leber congenital amaurosis.

Ophthalmic genetics·2006

Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1).

Ophthalmic genetics·2002

The ateliotic macula: a newly recognized developmental anomaly.

Transactions of the American Ophthalmological Society·2002

A case-control study of tobacco and alcohol consumption in Leber hereditary optic neuropathy.

American journal of ophthalmology·2000

Mutational analysis and clinical correlation in Leber congenital amaurosis.

Ophthalmic genetics·2000

Retinal detachment in Marfan syndrome.

Retina (Philadelphia, Pa.)·2000

No-History IOL Power Calculation After Myopic Laser Vision Correction: A Multicenter Retrospective Database Study of 14 Formulas With and Without Posterior Corneal Curvature.

American journal of ophthalmology·2026

Neighborhood Socioeconomic Deprivation and Adherence to Diabetic Retinopathy Screening Guidelines.

American journal of ophthalmology·2026

Optical coherence tomography-guided focal navigated laser photocoagulation in central serous chorioretinopathy: a non-inferiority study.

American journal of ophthalmology·2026

Glaucoma and Neurodegenerative Disease Risk: A 10-Year Assessment of Real-World Global Data.

American journal of ophthalmology·2026

Refining How We Diagnose and Classify Limbal Stem Cell deficiency.

American journal of ophthalmology·2026

Central Retinal Vessel Trunk Dragging in Highly Myopic Eyes.

American journal of ophthalmology·2026

Pili Annulati: A Case Series and Proposal for Classification.

Skin appendage disorders·2026

ß-Globin gene cluster haplotypes in Moroccan sickle cell disease patients: diversity pilot study.

African health sciences·2026

Deriving BMI-referenced, sex-specific fat mass index cutoff values in older Saudi adults: a cross-sectional secondary analysis.

Frontiers in nutrition·2026

Associations of intermediate hyperglycemia with elevated abdominal obesity, high-sensitivity C-reactive protein, and leptin in Korean adults.

Journal of Korean biological nursing science·2026

Child-to-adult body size trajectories and risk of rheumatoid arthritis: the mediating role of metabolic unhealthiness, low-grade inflammation, and the modifying effect of genetic susceptibility.

Journal of autoimmunity·2026

Bestrophinopathies: Clinical Characteristics, Natural History, and Genetic Landscape.

Ophthalmology. Retina·2026

Related Experiment Videos

Letter: Autosomal dominant inheritance in albinism

Related Concept Videos

A G1103R mutation in CRB1 is co-inherited with high hyperopia and Leber congenital amaurosis.

Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1).

The ateliotic macula: a newly recognized developmental anomaly.

A case-control study of tobacco and alcohol consumption in Leber hereditary optic neuropathy.

Mutational analysis and clinical correlation in Leber congenital amaurosis.

Retinal detachment in Marfan syndrome.

No-History IOL Power Calculation After Myopic Laser Vision Correction: A Multicenter Retrospective Database Study of 14 Formulas With and Without Posterior Corneal Curvature.

Neighborhood Socioeconomic Deprivation and Adherence to Diabetic Retinopathy Screening Guidelines.

Optical coherence tomography-guided focal navigated laser photocoagulation in central serous chorioretinopathy: a non-inferiority study.

Glaucoma and Neurodegenerative Disease Risk: A 10-Year Assessment of Real-World Global Data.

Refining How We Diagnose and Classify Limbal Stem Cell deficiency.

Central Retinal Vessel Trunk Dragging in Highly Myopic Eyes.

Pili Annulati: A Case Series and Proposal for Classification.

ß-Globin gene cluster haplotypes in Moroccan sickle cell disease patients: diversity pilot study.

Deriving BMI-referenced, sex-specific fat mass index cutoff values in older Saudi adults: a cross-sectional secondary analysis.

Associations of intermediate hyperglycemia with elevated abdominal obesity, high-sensitivity C-reactive protein, and leptin in Korean adults.

Child-to-adult body size trajectories and risk of rheumatoid arthritis: the mediating role of metabolic unhealthiness, low-grade inflammation, and the modifying effect of genetic susceptibility.

Bestrophinopathies: Clinical Characteristics, Natural History, and Genetic Landscape.

Related Experiment Videos

Letter: Autosomal dominant inheritance in albinism

Related Concept Videos

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