- ►nih.gov [PDF] CI Hope, S Bundey, D Proops, AR Fielder - British Journal of Ophthalmology, 1997 - bjo.bmj.com METHODS Symptomatic cases of Usher syndrome (US) resident in the city of
Birmingham in June 1994 were ascertained through multiple sources. Ophthalmic
and audiological reassessment together with examination of medical records ... Cited by 54 - Related articles - BL Direct - All 7 versions
T Rosenberg, M Haim, AM Hauch, A Parving - Clinical genetics, 1997 - interscience.wiley.com The study was undertaken to procure population-based prevalence data on the
various types of Usher syndrome and other retinal dystrophy-hearing impairment
associations. The medical files on 646 patients with a panretinal ... Cited by 61 - Related articles - BL Direct - All 3 versions
- ►nih.gov [PDF] XZ Liu, C Hope, CY Liang, JM Zou, LR Xu, T … - The American Journal of Human Genetics, 1999 - Elsevier Usher syndrome (USH), an autosomal recessive condition, is characterized by
hearing impairment associated with retinitis pigmentosa (RP). It is a clinically
and genetically heterogeneous condition. Three clinical forms of USH have ... Cited by 39 - Related articles - BL Direct - All 7 versions
L Pakarinen, S Karjalainen, KOJ Simola, P … - Laryngoscope, 1995 - interscience.wiley.com Usher's syndrome, type 3 (USH3) is characterized by progressive hearing loss.
Usher's syndrome, type 3 has been supposed to be rare, occurring in 2% to 4% of
all patients with Usher's syndrome. In a nationwide study we collected data ... Cited by 43 - Related articles - BL Direct - All 3 versions
ET Tsilou, BI Rubin, RC Caruso, GF Reed, A … - Acta Ophthalmologica Scandinavica, 2002 - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 23 - Related articles - BL Direct - All 3 versions
RJH Smith, CI Berlin, JF Hejtmancik, BJB … - American journal of medical genetics, 1994 - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 159 - Related articles - BL Direct - All 3 versions
- ►nih.gov MD Weston, JD Eudy, S Fujita, SF Yao, S … - The American Journal of Human Genetics, 2000 - Elsevier Usher syndrome type IIa (USHIIa) is an autosomal recessive disorder
characterized by moderate to severe sensorineural hearing loss and progressive
retinitis pigmentosa. This disorder maps to human chromosome 1q41. ... Cited by 78 - Related articles - BL Direct - All 8 versions
A Nuutila - Journal de génétique humaine, 1970 - ncbi.nlm.nih.gov 1: J Genet Hum. 1970 May;18(1):57-88. Dystrophia retinae pigmentosa--dysacusis syndrome
(DRD): a study of the Usher- or Hallgren syndrome. Nuutila A. ... Cited by 68 - Related articles
J Grondahl - Clin Genet, 1987 - interscience.wiley.com Retinitis pigmentosa was diagnosed in 101 persons from 53 families. The
prognosis for visual function was most favourable for the autosomal dominant
group (38 patients from 8 families). The autosomal recessive group (40 ... Cited by 41 - Related articles - All 4 versions
- ►cell.com XZ Liu, C Hope, J Walsh, V Newton, XM Ke, … - The American Journal of Human Genetics, 1998 - Elsevier Usher syndrome (USH) is the most common recessive syndromic hearing loss
characterized by congenital hearing impairment associated with retinitis
pigmentosa (RP). It is a clinically and genetically heterogeneous ... Cited by 60 - Related articles - BL Direct - All 9 versions
