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Publications by Jill Clayton-Smith

Bi-Allelic Loss-Of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

American Journal of Human Genetics

English

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

American Journal of Human Genetics

English

Heterozygous Loss-Of-Function Variants of MEIS2 Cause a Triad of Palatal Defects, Congenital Heart Defects, and Intellectual Disability

European Journal of Human Genetics

English

Brittle Cornea Syndrome: Recognition, Molecular Diagnosis and Management

Orphanet Journal of Rare Diseases

English

Relationship of Child IQ to Parental IQ and Education in Children With Fetal Antiepileptic Drug Exposure

Epilepsy and Behavior

Behavioral Neuroscience

English

Cognitive Function at 3 Years of Age After Fetal Exposure to Antiepileptic Drugs

New England Journal of Medicine

English