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Integration of individualized and population-level molecular epidemiology data to model COVID-19 outcomes.
Site of disease and treatment protocol as correlates of swallowing function in patients with head and neck cancer treated with chemoradiation.
Clinical and molecular basis of classical lissencephaly: Mutations in the LIS1 gene (PAFAH1B1).
De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome.
Genetic links between brain development and brain evolution.
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Genetic links between brain development and brain evolution.
Genetic links between brain development and brain evolution. Nat Rev Genet. 2005 Jul; 6(7):581-90.
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PubMed
subject areas
Animals
Brain
Evolution, Molecular
Humans
Microcephaly
Nerve Tissue Proteins
Phylogeny
authors with profiles
William B. Dobyns