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Publications by J. C K Barber
Medical Genetics: Advances in Brief: Digenic Retinitis Pigmentosa Due to Mutations at the Unlinked Peripherin/RDS and ROM1 Loci
Journal of Medical Genetics
Genetics
Medical Genetics: Advances in Brief: Duplication in the Hypoxanthine Phosphoribosyl-Transferase Gene Caused by Alu-Alu Recombination in a Patient With Lesch-Nyhan Syndrome
Journal of Medical Genetics
Genetics
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Retinitis Pigmentosa Families Showing Apparent X Linked Inheritance but Unlinked to the RP2 or RP3 Loci.
Journal of Medical Genetics
Genetics
Medical Genetics: Advances in Brief
Journal of Medical Genetics
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Medical Genetics: Advances in Brief
Journal of Medical Genetics
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Advances in the Understanding of Retinitis Pigmentosa
Eye
Medicine
Arts
Sensory Systems
Ophthalmology
Humanities
Medical Genetics: Advances in Brief: Familial Intracranial Aneurysms
Journal of Medical Genetics
Genetics
Rhodopsin Mutations in Chinese Patients With Retinitis Pigmentosa
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Medical Genetics: Advances in Brief: Editorial: Our Educational Challenge
Journal of Medical Genetics
Genetics
