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Publications by Tiffany Lynn Newton
Mutations in RAI1 Associated With Smith–Magenis Syndrome
Nature Genetics
Genetics
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Auditory Phenotype of Smith–Magenis Syndrome
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Cognitive Functioning in Children and Adults With Smith-Magenis Syndrome
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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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Smith-Magenis Syndrome: Clinical Evaluation in Seven Brazilian Patients
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Reversed Gender Ratio of Autism Spectrum Disorder in Smith-Magenis Syndrome
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Molecular Screening for Smith-Magenis Syndrome Among Patients With Mental Retardation of Unknown Cause
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Smith-Magenis Syndrome: A New Contiguous Gene Syndrome. Report of Three New Cases.
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Circadian Abnormalities in Mouse Models of Smith-Magenis Syndrome: Evidence for Involvement ofRAI1
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OP08.05: Prenatal Diagnosis of Smith-Magenis Syndrome in Fetus With Mild Unilateral Borderline Ventriculomegaly: A Case Report
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