Literature DB >> 5937908

The hereditary syndrome of congenital deafness and retinitis pigmentosa. (Usher's syndrome).

H W Kloepfer, J K Laguaite.   

Abstract

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Year:  1966        PMID： 5937908     DOI： 10.1288/00005537-196605000-00004

Source DB:  PubMed          Journal:  Laryngoscope        ISSN： 0023-852X            Impact factor:   3.325


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  5 in total

1.  Usher syndrome in the city of Birmingham--prevalence and clinical classification.

Authors:  C I Hope; S Bundey; D Proops; A R Fielder
Journal:  Br J Ophthalmol       Date:  1997-01       Impact factor: 4.638

Review 2.  Inherited diseases of the inner ear in man in the light of studies on the mouse.

Authors:  M S Deol
Journal:  J Med Genet       Date:  1968-06       Impact factor: 6.318

3.  Congenital mirror movements.

Authors:  G D Schott; M A Wyke
Journal:  J Neurol Neurosurg Psychiatry       Date:  1981-07       Impact factor: 10.154

4.  Dark adaptation testing in heterozygotes of Usher's syndrome.

Authors:  S Sondheimer; G A Fishman; R S Young; V A Vasquez
Journal:  Br J Ophthalmol       Date:  1979-08       Impact factor: 4.638

5.  Peripheral Anomalies in USH2A Cause Central Auditory Anomalies in a Mouse Model of Usher Syndrome and CAPD.

Authors:  Peter A Perrino; Dianne F Newbury; R Holly Fitch
Journal:  Genes (Basel)       Date:  2021-01-24       Impact factor: 4.096
  5 in total

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