Bilateral Complete Labyrinthine Aplasia With Bilateral Internal Carotid Artery Aplasia, Developmental Delay, and Gaze Abnormalities: A Presumptive Case of a Rare HOXA1 Mutation Syndrome
American Journal of Neuroradiology - United States
doi 10.3174/ajnr.a1969
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Date
January 14, 2010
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American Society of Neuroradiology (ASNR)