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Publications by CHRIS F. INGLEHEARN

Meiotic Drive at the Myotonic Dystrophy and the Cone-Rod Dystrophy Loci on Chromosome 19q13.3

American Journal of Human Genetics

English

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Spondylometaphyseal Dysplasia-Cone-Rod Dystrophy Syndrome

English

Identification of a Locus on Chromosome 2q11 at Which Recessive Amelogenesis Imperfecta and Cone-Rod Dystrophy Cosegregate

European Journal of Human Genetics

English

Novel C8ORF37 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica

English

Myotonic Dystrophy and the Heart

English

Novel CDHR1 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica

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Rod-Cone Dystrophy in Spinocerebellar Ataxia Type 1

Archives of Ophthalmology

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Autosomal Dominant Cone-Rod Dystrophy With Negative Electroretinogram.

British Journal of Ophthalmology

Molecular Neuroscience

Sensory Systems

English

Myotonic Dystrophy and Thymoma.

Journal of Neurology, Neurosurgery and Psychiatry

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Myotonic Dystrophy Type 1

English