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Publications by J L Struthers

Molecular Screening for Smith-Magenis Syndrome Among Patients With Mental Retardation of Unknown Cause

Journal of Medical Genetics

English

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Smith-Magenis Syndrome: Clinical Evaluation in Seven Brazilian Patients

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Auditory Phenotype of Smith–Magenis Syndrome

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Mutations in RAI1 Associated With Smith–Magenis Syndrome

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Cognitive Functioning in Children and Adults With Smith-Magenis Syndrome

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A Spatial Analysis of Mental Retardation of Unknown Cause and Maternal Residence During Pregnancy

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Molecular Analysis of the Retinoic Acid Induced 1 Gene (RAI1) in Patients With Suspected Smith-Magenis Syndrome Without the 17p11.2 Deletion

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Circadian Abnormalities in Mouse Models of Smith-Magenis Syndrome: Evidence for Involvement ofRAI1

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A New Strategy for Cryptic Telomeric Translocation Screening in Patients With Idiopathic Mental Retardation.

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Smith-Magenis Syndrome: A New Contiguous Gene Syndrome. Report of Three New Cases.

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