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0011110995
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Retinitis pigmentosa and allied diseases
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Pearson K. (ed.). London, Cambridge University Press
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Bell, J.1
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2
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0020619770
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Usher syndrome: Definition and estimate of prevalence from two high-risk populations
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BOUGHMAN J., VERNON M. and SHAVER K.: Usher syndrome: definition and estimate of prevalence from two high-risk populations. J. Chronic. Dis., 1983, 36, 595-603.
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3
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0019197202
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The effects of typical retinitis pigmentosa, Leber congenital amaurosis, centro-peripheral dystrophy, and Usher syndrome on educational and vocational success and personality development
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COOKER STOGNER P.: The effects of typical retinitis pigmentosa, Leber congenital amaurosis, centro-peripheral dystrophy, and Usher syndrome on educational and vocational success and personality development. Int. J. Rehab. Research, 1980, 3, 3, 357-366.
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DAVENPORT S.L. H.: Improving communication with the Deaf patient. J. Family Practice, 1977, 4, 6, 1065-1068.
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A five-State study of Usher syndrome: Incidence & Service Implications
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May
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ENGLISH J.: A five-State study of Usher syndrome: Incidence & Service Implications. A. A. D., May 1978, 360-364.
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English, J.1
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6
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0019615093
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Media and Instructoral Techniques for Usher Syndrome
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September
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FISCHER C.: Media and Instructoral Techniques for Usher Syndrome. A. A. D., 126, September 1981, 582-586.
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Fischer, C.1
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Usher syndrome. Ophthalmic and neuro-otologic findings suggesting genetic heterogeneity
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FISHMAN G.A., KUMAR A., TOROK J. and ANDERSON R. J.: Usher syndrome. Ophthalmic and neuro-otologic findings suggesting genetic heterogeneity. Arch. Ophthalmol, 1983, 101, 1367-1374.
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0023091261
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Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in Norway
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GROND AHL J.: Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in Norway. Clin. Genet., 1987, 31, 255-264.
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Grondahl, J.1
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9
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7944229728
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Retinitis pigmentosa combined with congenital deafness; with vesti-bulo-cerebellar ataxia and mental abnormality in a proportion of cases: A clinical and genetico-statistical study
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HALLOREN B.: Retinitis pigmentosa combined with congenital deafness; with vesti-bulo-cerebellar ataxia and mental abnormality in a proportion of cases: a clinical and genetico-statistical study. Acta Psychiatr. Scand., 1959, 34 (Suppl. 138), 5-101.
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Usher syndrome: Programmatic Considerations
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HICKS D. E.; Usher syndrome: Programmatic Considerations. A.A. D., May 1978, 365-371.
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0019503642
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The Usher Syndrome Adolescent: Programming Implications for School Administrators, Teachers, and Residential Advisors
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June
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HICKS W. M. and HICKS D. E.: The Usher Syndrome Adolescent: Programming Implications for School Administrators, Teachers, and Residential Advisors. A.A D., June 1981, 126, 422-431.
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12
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Usher's syndrome type III: ENG findings in four affected and six unaffected siblings
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KARJALAINEN S., TERSVIRTA M., KARJA J. and KARJALAINEN H.: Usher's syndrome type III: ENG findings in four affected and six unaffected siblings. J. Laryngol. Oto. 1985, 94, 43-48.
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Karjalainen, S.1
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Gene mapping of Usher syndrome type IIa: Localization of the Gene to a 2.1 cM segment on chromosome 1q41
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KIMBERLING W.J., WESTON M.D., MOLLER C.G., AAREM A., CREMERS C.W., SUMEGI J., ING P., CONNOLLY C., MARTINI A., MILANI M., TAMAYO M.L., BERNAL J., GREENBERG J., and AYUSO C.: Gene mapping of Usher syndrome type IIa: Localization of the Gene to a 2.1 cM segment on chromosome 1q41. Am. J. Hum. Genet, 1995, 56, 216-223.
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Kimberling, W.J.1
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0002318769
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Abkunft aus Ehen unter Blutsverwandten als grund von Retinitis pigmentosa
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LIEBREICH R.: Abkunft aus Ehen unter Blutsverwandten als grund von Retinitis pigmentosa. Dtsch Klin., 1861, 1, 53-55.
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Liebreich, R.1
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Dystrophia retinae pigtnentosa-dysacusis syndrome (DRD): A study of the Usher or Hallgren syndrome
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NUUTILA A.: Dystrophia retinae pigtnentosa-dysacusis syndrome (DRD): a study of the Usher or Hallgren syndrome. J. Genet. Hum., 1970, 18, 57-88.
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Nuutila, A.1
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Neuroradiology and clinical aspects of Usher syndrome
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Accepted 1996
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TAMAYO M.L., MALDONADO C., PLAZA S., ALVIRA G.M., TAMAYO G.E., ZAMBRANO M., PRIAS J.L., and BERNAL J.E.: Neuroradiology and clinical aspects of Usher syndrome. Clin Genet., 1996, 49, 00-00 (Accepted 1996).
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19
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Usher syndrome: Results of a screening program in Colombia
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TAMAYO M.L., BERNAL I.E., TAMAYO G., FRIAS J.L., ALVIRA G., VERGARA O., RODRIGUEZ V., URIBE J.I. and SILVA J.C.: Usher syndrome: results of a screening program in Colombia. Clin. Genet., 1991, 40, 304-311.
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Tamayo, M.L.1
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Study of the etiology of deafness in an institutionalized population in Colombia
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TAMAYO M.L., BERNAL J.E., TAMAYO G. and PRIAS J.L.: Study of the etiology of deafness in an institutionalized population in Colombia. Am. J. Med. Genet., 1992, 44, 405-408.
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Tamayo, M.L.1
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Prias, J.L.4
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Families of Adolescent Children with Usher Syndrome: Developing Services to Meet their Needs
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TORRIE C.: Families of Adolescent Children with Usher Syndrome: Developing Services to Meet their Needs. A.A.D., May 1978, 381-388.
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On the inheritance of retinitis pigmentosa, with notes of cases
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USHER Ch.: On the inheritance of retinitis pigmentosa, with notes of cases. R. Lond. Ophthal. Hosp. Rep., 1914, 19, 130-256.
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Usher Syndrome-Deafness and progressive blindness. Clinical cases, prevention, theory and literature survey
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VERNON M.: Usher Syndrome-Deafness and progressive blindness. Clinical cases, prevention, theory and literature survey. J. Chron. Dis., 1969, 22, 133-151.
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Vereinzelte Beobachtungen und Bemerkungen: Exceptionelles Verhalten des Gesichtfeldes bei Pigmententartung der Netzhaut
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