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Publications by William B. Dobyns
MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon Guidance
American Journal of Human Genetics
Genetics
Hypomorphic Recessive Variants in SUFU Impair the Sonic Hedgehog Pathway and Cause Joubert Syndrome With Cranio-Facial and Skeletal Defects
American Journal of Human Genetics
Genetics
De Novo Variants in WDR37 Are Associated With Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia
American Journal of Human Genetics
Genetics
Somatic PDGFRB Activating Variants in Fusiform Cerebral Aneurysms
American Journal of Human Genetics
Genetics
Association ofMTORMutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism
JAMA Neurology
Neurology
Characterizing the Pattern of Anomalies in Congenital Zika Syndrome for Pediatric Clinicians
JAMA Pediatrics
Child Health
Pediatrics
Perinatology
Comparison of Brain MRI Findings With Language and Motor Function in the Dystroglycanopathies
Neurology
Neurology
Anatomical Configurations Associated With Posthemorrhagic Hydrocephalus Among Premature Infants With Intraventricular Hemorrhage
Neurosurgical Focus
Medicine
Surgery
Neurology
Molecular and Neuroimaging Findings in Pontocerebellar Hypoplasia Type 2 (PCH2): Is Prenatal Diagnosis Possible?
American Journal of Medical Genetics, Part A
Genetics
Unbalanced Der(5)t(5;20) Translocation Associated With Megalencephaly, Perisylvian Polymicrogyria, Polydactyly and Hydrocephalus
American Journal of Medical Genetics, Part A
Genetics
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