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History (11)
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations.
Automated recognition of bird song elements from continuous recordings using dynamic time warping and hidden Markov models: a comparative study.
Seeking the Amygdala: Novel Use of Diffusion Tensor Imaging to Delineate the Basolateral Amygdala.
Expanding the SHOC2 mutation associated phenotype of Noonan syndrome with loose anagen hair: structural brain anomalies and myelofibrosis.
Congenital pontocerebellar atrophy in three patients: clinical, radiologic and etiologic considerations.
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Congenital pontocerebellar atrophy in three patients: clinical, radiologic and etiologic considerations.
Congenital pontocerebellar atrophy in three patients: clinical, radiologic and etiologic considerations. Neuroradiology. 1996 Oct; 38(7):684-7.
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PubMed
subject areas
Cerebellum
Chromosome Aberrations
Chromosome Disorders
Diseases in Twins
Female
Follow-Up Studies
Genes, Recessive
Humans
Infant
Infant, Newborn
Magnetic Resonance Imaging
Neurologic Examination
Olivopontocerebellar Atrophies
Pons
Twins, Monozygotic
authors with profiles
William B. Dobyns