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Updated: Jul 27, 2026

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Mouse Eye Enucleation for Remote High-throughput Phenotyping
Published on: November 19, 2011
Familial congenital monochromatism, cataracts, and sensorineural deafness
American Journal of Diseases of Children (1960)
|December 1, 1976
Abstract:
Two sisters had diagnoses of congenital monochromatism, cataracts, bilateral nonprogressive sensorineural deafness, and hyperinsulinism in both, and labyrinthine dysfunction in one. This recessively inherited condition is added to the growing number of syndromes in which one of the features may be a disturbance of hypothalamic function.
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