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Publications by M al-Maghtheh
Bimodal Expressivity in Dominant Retinitis Pigmentosa Genetically Linked to Chromosome 19q.
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
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Autosomal Dominant Retinitis Pigmentosa: A New Multi-Allelic Marker (D3S621) Genetically Linked to the Disease Locus (RP4)
Human Genetics
Genetics
Phenotype-Genotype Correlations in X Linked Retinitis Pigmentosa.
Journal of Medical Genetics
Genetics
Presence of a Triple Concentric Autofluorescence Ring inNR2E3-p.G56R–Linked Autosomal Dominant Retinitis Pigmentosa (ADRP)
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
X-Linked Intellectual Disability-Retinitis Pigmentosa Syndrome
Linkage of Internal Minisatellite Loci on Chromosome 1 and Exclusion of Autosomal Dominant Retinitis Pigmentosa Proximal to Rhesus.
Journal of Medical Genetics
Genetics
Severe Manifestations in Carrier Females in X Linked Retinitis Pigmentosa.
Journal of Medical Genetics
Genetics
Phenotype-Genotype Correlations in Autosomal Dominant Retinitis Pigmentosa Caused by RHO, D190N
Current Eye Research
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Difference Between RP2 and RP3 Phenotypes in X Linked Retinitis Pigmentosa
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Abnormal Dark Adaptation Kinetics in Autosomal Dominant Sector Retinitis Pigmentosa Due to Rod Opsin Mutation.
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular