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Gao Y 16

Showing records 1 to 16 | Display all abstracts from Gao Y

99383 A Novel Mutation in the Membrane Frizzled-Related Protein Gene for Posterior Microphthalmia, Non-pigmented Retinitis Pigmentosa, Optic Nerve Drusen, and Retinoschisis in a Consanguineous Family
Ren X
Frontiers in medicine 2022; 9: 835621
99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Zhong Z; Ding J
Ophthalmology 2022; 129: 821-828
99383 A Novel Mutation in the Membrane Frizzled-Related Protein Gene for Posterior Microphthalmia, Non-pigmented Retinitis Pigmentosa, Optic Nerve Drusen, and Retinoschisis in a Consanguineous Family
Gao Y
Frontiers in medicine 2022; 9: 835621
99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Su G
Ophthalmology 2022; 129: 821-828
99383 A Novel Mutation in the Membrane Frizzled-Related Protein Gene for Posterior Microphthalmia, Non-pigmented Retinitis Pigmentosa, Optic Nerve Drusen, and Retinoschisis in a Consanguineous Family
Lin Y
Frontiers in medicine 2022; 9: 835621
99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Liao W
Ophthalmology 2022; 129: 821-828
99383 A Novel Mutation in the Membrane Frizzled-Related Protein Gene for Posterior Microphthalmia, Non-pigmented Retinitis Pigmentosa, Optic Nerve Drusen, and Retinoschisis in a Consanguineous Family
Fu X
Frontiers in medicine 2022; 9: 835621
99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Gao Y
Ophthalmology 2022; 129: 821-828
99383 A Novel Mutation in the Membrane Frizzled-Related Protein Gene for Posterior Microphthalmia, Non-pigmented Retinitis Pigmentosa, Optic Nerve Drusen, and Retinoschisis in a Consanguineous Family
Xiao L
Frontiers in medicine 2022; 9: 835621
99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Zhu Y
Ophthalmology 2022; 129: 821-828
99383 A Novel Mutation in the Membrane Frizzled-Related Protein Gene for Posterior Microphthalmia, Non-pigmented Retinitis Pigmentosa, Optic Nerve Drusen, and Retinoschisis in a Consanguineous Family
Wang X
Frontiers in medicine 2022; 9: 835621
99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Deng Y
Ophthalmology 2022; 129: 821-828
99383 A Novel Mutation in the Membrane Frizzled-Related Protein Gene for Posterior Microphthalmia, Non-pigmented Retinitis Pigmentosa, Optic Nerve Drusen, and Retinoschisis in a Consanguineous Family
Zeng Z; Bao L
Frontiers in medicine 2022; 9: 835621
99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Li F; Du L
Ophthalmology 2022; 129: 821-828
99383 A Novel Mutation in the Membrane Frizzled-Related Protein Gene for Posterior Microphthalmia, Non-pigmented Retinitis Pigmentosa, Optic Nerve Drusen, and Retinoschisis in a Consanguineous Family
Yan N; Zhang M; Tang L
Frontiers in medicine 2022; 9: 835621
99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Yang P
Ophthalmology 2022; 129: 821-828

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