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Publications by Gary D. Clark

Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome With Intellectual Disability and Developmental Delay

American Journal of Human Genetics
Genetics
2019English

IRF2BPL Is Associated With Neurological Phenotypes

American Journal of Human Genetics
Genetics
2018English

De Novo Variants in WDR37 Are Associated With Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

American Journal of Human Genetics
Genetics
2019English

Bi-Allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes

American Journal of Human Genetics
Genetics
2019English

Open-Label Use of Highly* Purified CBD (Epidiolex®) in Patients With CDKL5 Deficiency Disorder and Aicardi, Dup15q, and Doose Syndromes

Epilepsy and Behavior
NeurologyBehavioral Neuroscience
2018English

Bilateral in Utero Cerebellar Infarction

Journal of Child Neurology
Child HealthNeurologyPediatricsPerinatology
2011English

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