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Publications by Gerald F. Cox

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

Multidisciplinary

English

Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome

American Journal of Human Genetics

English

Related publications

Mutations in RAI1 Associated With Smith–Magenis Syndrome

Nature Genetics

English

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

Journal of Medical Genetics

English

Smith-Magenis Syndrome: Clinical Evaluation in Seven Brazilian Patients

Genetics and Molecular Research

Molecular Biology

English

Auditory Phenotype of Smith–Magenis Syndrome

Journal of Speech, Language, and Hearing Research

English

Structure and Evolution of the Smith-Magenis Syndrome Repeat Gene Clusters, SMS-REPs

Genome Research

English

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

Journal of Medical Genetics

English

Cognitive Functioning in Children and Adults With Smith-Magenis Syndrome

European Journal of Medical Genetics

English

Genomic Organisation of the ∼1.5 Mb Smith-Magenis Syndrome Critical Interval: Transcription Map, Genomic Contig, and Candidate Gene Analysis

European Journal of Human Genetics

English

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

Molecular Autism

Developmental Neuroscience

Developmental Biology

Molecular Biology

English