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Publications by Joseph H Hersh

725 a New Syndrome of Retinitis Pigmentosa, Hearing Loss, Mental Retardation, and Dysmorphology

Pediatric Research

English

Expanding the Clinical Phenotype of the 3q29 Microdeletion Syndrome and Characterization of the Reciprocal Microduplication

Molecular Cytogenetics

Molecular Medicine

Molecular Biology

English

Related publications

Giant Retinal Tear and Retinal Detachment With Underlying Retinitis Pigmentosa and Hearing Loss

Sensory Systems

English

Posterior Column Ataxia-Retinitis Pigmentosa Syndrome

English

Missense Mutation in the USH2A Gene: Association With Recessive Retinitis Pigmentosa Without Hearing Loss

American Journal of Human Genetics

English

Brachydactyly-Short Stature-Retinitis Pigmentosa Syndrome

English

Retinitis Pigmentosa-Intellectual Disability-Deafness-Hypogonadism Syndrome

English

Retinitis Pigmentosa, Hypertension, and Uraemia in Werner's Syndrome

English

X-Linked Intellectual Disability-Retinitis Pigmentosa Syndrome

English

C-Reactive Protein and Progression of Vision Loss in Retinitis Pigmentosa

Acta Ophthalmologica

English

The R245X Mutation of PCDH15 in Ashkenazi Jewish Children Diagnosed With Nonsyndromic Hearing Loss Foreshadows Retinitis Pigmentosa

Pediatric Research

English