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1992 | 1 |
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Gene mapping of the Usher syndromes.
Otolaryngol Clin North Am. 1992 Oct;25(5):923-34.
Otolaryngol Clin North Am. 1992.
PMID: 1408196
Review.
Persons with type I do not find hearing aids useful, have delayed motor development, and experience progressive night blindness and peripheral visual loss, which usually begins in their second decade. ...Persons with USH2 find hearing aids beneficial, have no …
Persons with type I do not find hearing aids useful, have delayed motor development, and experience progressive night blind …
Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.
Lewis RA, Otterud B, Stauffer D, Lalouel JM, Leppert M.
Lewis RA, et al.
Genomics. 1990 Jun;7(2):250-6. doi: 10.1016/0888-7543(90)90547-8.
Genomics. 1990.
PMID: 1971808
Usher syndrome is a heterogeneous group of autosomal recessive disorders that combines variably severe congenital neurosensory hearing impairment with progressive night-blindness and visual loss similar to that in retinitis pigmentosa. ...
Usher syndrome is a heterogeneous group of autosomal recessive disorders that combines variably severe congenital neurosensory hearing impai …
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