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Publications by Weiping Wu

A New 2–Base Pair Deletion in the RPGR Gene in a Black Family With X-Linked Retinitis Pigmentosa

Archives of Ophthalmology

English

Related publications

Mutation Analysis of the RPGR Gene Reveals Novel Mutations in South European Patients With X-Linked Retinitis Pigmentosa

European Journal of Human Genetics

English

Phenotype-Genotype Correlations in X Linked Retinitis Pigmentosa.

Journal of Medical Genetics

English

X-Linked Intellectual Disability-Retinitis Pigmentosa Syndrome

English

Severe Manifestations in Carrier Females in X Linked Retinitis Pigmentosa.

Journal of Medical Genetics

English

Difference Between RP2 and RP3 Phenotypes in X Linked Retinitis Pigmentosa

British Journal of Ophthalmology

Molecular Neuroscience

Sensory Systems

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Correction:Unilateral Retinitis Pigmentosa Occurring in an Individual With a Mutation in the CLRN1 Gene

BMJ Case Reports

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A Novel NR2E3 Gene Mutation in Autosomal Recessive Retinitis Pigmentosa With Cystic Maculopathy

Acta Ophthalmologica

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Polypoidal Choroidal Vasculopathy in a Case With Retinitis Pigmentosa

International Ophthalmology

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Spectral-Domain Optical Coherence Tomography Measures of Outer Segment Layer Progression in Patients With X-Linked Retinitis Pigmentosa

JAMA Ophthalmology

English