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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.
Memories of the McNutt fellowship.
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Memories of the McNutt fellowship.
Memories of the McNutt fellowship. J Cutan Pathol. 2008 Nov; 35 Suppl 2:iv-vi.
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PubMed
subject areas
Dermatology
Fellowships and Scholarships
Pathology, Clinical
authors with profiles
Christopher Shea