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Publications by Rebecca E. Slager

Mutations in RAI1 Associated With Smith–Magenis Syndrome

Nature Genetics

English

Related publications

Auditory Phenotype of Smith–Magenis Syndrome

Journal of Speech, Language, and Hearing Research

English

Cognitive Functioning in Children and Adults With Smith-Magenis Syndrome

European Journal of Medical Genetics

English

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

Multidisciplinary

English

Smith-Magenis Syndrome: Clinical Evaluation in Seven Brazilian Patients

Genetics and Molecular Research

Molecular Biology

English

Reversed Gender Ratio of Autism Spectrum Disorder in Smith-Magenis Syndrome

Molecular Autism

Developmental Neuroscience

Developmental Biology

Molecular Biology

English

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

Journal of Medical Genetics

English

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

Journal of Medical Genetics

English

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

American Journal of Medical Genetics, Part A

English

OP08.05: Prenatal Diagnosis of Smith-Magenis Syndrome in Fetus With Mild Unilateral Borderline Ventriculomegaly: A Case Report

Ultrasound in Obstetrics and Gynecology

Nuclear Medicine

Ultrasound Technology

Reproductive Medicine

English