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Gao Y 18

Showing records 1 to 18 | 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

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99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Zhong Z
Ophthalmology 2022; 129: 821-828

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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

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99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Ding J; Su G
Ophthalmology 2022; 129: 821-828

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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

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99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Liao W
Ophthalmology 2022; 129: 821-828

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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

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99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Gao Y
Ophthalmology 2022; 129: 821-828

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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

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99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Zhu Y
Ophthalmology 2022; 129: 821-828

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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

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99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Deng Y
Ophthalmology 2022; 129: 821-828

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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
Frontiers in medicine 2022; 9: 835621

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99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Li F
Ophthalmology 2022; 129: 821-828

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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
Bao L; Yan N
Frontiers in medicine 2022; 9: 835621

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99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Du L
Ophthalmology 2022; 129: 821-828

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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
Zhang M; Tang L
Frontiers in medicine 2022; 9: 835621

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99166 Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
Yang P
Ophthalmology 2022; 129: 821-828

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