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Publications by Jamel Chelly
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder
American Journal of Human Genetics
Genetics
Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation
American Journal of Human Genetics
Genetics
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder
American Journal of Human Genetics
Genetics
Correction To: The Landscape of Epilepsy-Related GATOR1 Variants
Genetics in Medicine
Medicine
Genetics
Correction: Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
A Missense Mutation Within the Fork-Head Domain of the Forkhead Box G1 Gene (FOXG1) Affects Its Nuclear Localization
Human Mutation
Genetics
Mild Malformations of Cortical Development in Sleep-Related Hypermotor Epilepsy Due to KCNT1 Mutations
Annals of Clinical and Translational Neurology
Neuroscience
Neurology
Mutations in the ZNF41 Gene Are Associated With Cognitive Deficits: Identification of a New Candidate for X-Linked Mental Retardation
American Journal of Human Genetics
Genetics
Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated With Mental Retardation
American Journal of Human Genetics
Genetics
A New Chromosome X Exon-Specific Microarray Platform for Screening of Patients With X-Linked Disorders
Journal of Molecular Diagnostics
Forensic Medicine
Pathology
Molecular Medicine
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