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Mutations in KATNB1 cause complex cerebral malformations by disrupting asymmetrically dividing neural progenitors.
Beta-myosin heavy chain gene mutations in familial hypertrophic cardiomyopathy: the usual suspect?
Patterns of failure, prognostic factors and survival in locoregionally advanced head and neck cancer treated with concomitant chemoradiotherapy: a 9-year, 337-patient, multi-institutional experience.
Perspectives on combination chemotherapy with concomitant radiotherapy for poor-prognosis head and neck cancer.
Defining the phenotypical spectrum associated with variants in TUBB2A.
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Defining the phenotypical spectrum associated with variants in TUBB2A.
Defining the phenotypical spectrum associated with variants in TUBB2A. J Med Genet. 2021 01; 58(1):33-40.
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PubMed
subject areas
Adolescent
Adult
Brain
Cerebellar Vermis
Child
Child, Preschool
Developmental Disabilities
Female
Genetic Predisposition to Disease
Humans
Intellectual Disability
Male
Mutation, Missense
Nervous System Malformations
Neuroimaging
Phenotype
Polymicrogyria
Tubulin
Young Adult
authors with profiles
William B. Dobyns