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Fan B 24
Showing records 1 to 24 | Display all abstracts from Fan B98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Collantes ERA
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Simcoe MJ
Ophthalmology 2022; 129: 626-636
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Delfin MS
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Shah A; Fan B
Ophthalmology 2022; 129: 626-636
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Fan B; Torregosa JMR
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Choquet H
Ophthalmology 2022; 129: 626-636
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Siguan-Bell C
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Weisschuh N
Ophthalmology 2022; 129: 626-636
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Florcruz NVG
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Waseem NH
Ophthalmology 2022; 129: 626-636
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Martinez JMD
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Jiang C; Melles RB
Ophthalmology 2022; 129: 626-636
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Masna-Hidalgo BJ; Guzman VPT
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Ritch R; Mahroo OA
Ophthalmology 2022; 129: 626-636
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Anotado-Flores JF; Levina FD
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Wissinger B; Jorgenson E
Ophthalmology 2022; 129: 626-636
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Hernandez SRC
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Wiggs JL
Ophthalmology 2022; 129: 626-636
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Collantes AA
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Garway-Heath DF
Ophthalmology 2022; 129: 626-636
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Sibulo MC; Rong S
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Hysi PG
Ophthalmology 2022; 129: 626-636
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Wiggs JL
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Hammond CJ
Ophthalmology 2022; 129: 626-636
