![]() ![]() Hereditary Hearing Loss Homepage: uia.ac.be/dnalab/hhhĪlagramam, K.N., Murcia, C.L., Kwon, H.Y., et al., The Mouse Ames Waltzer Hearing-Loss Mutant Is Caused by Mutation of Pcdh15, a Novel Protocadherin Gene, Nat. Wayne, S., Lowry, R.B., McLeod, D.R., et al., Localization of the Usher Syndrome Type 1F (Ush1F) to Chromosome 10, Am. 103–107.Ĭhaib, H., Kaplan, J., Gerber, S., et al., A Newly Identified Locus for Usher Syndrome Type I, USH1E, Maps to Chromosome 21q21, Hum. 1689–1692.ĭi Palma, F., Holme, R.H., Bryda, E.C., et al., Mutations in Cdh23, Encoding a New Type of Cadherin, Cause Stereocilia Disorganization in Waltzer, the Mouse Model for Usher Syndrome Type 1D, Nat. Localization of the Usher Syndrome Type 1D Gene ( Ush1D) to Chromosome 10, Hum. Wayne, S., Der Kaloustian V.M., Schloss M., et al. Johnson, K.R., Gagnon, L.H., Webb, L.S., et al., Mouse Models of USH1C and DFNB18: Phenotypic and Molecular Analyses of Two New Spontaneous Mutations of the Ush1c Gene, Hum. Liu, X.Z., Newton, V.E., Steel, K.P., et al., Identification of a New Mutation of the Myosin VII Head Region in Usher Syndrome Type 1, Hum. Gibson, F., Walsh, J., Mburu, P., et al., A Type VII Myosin Encoded by the Mouse Deafness Gene shaker-1, Nature, 1995, no. 988–994.Īstuto, L.M., Weston, M.D., Carney, C.A., et al., Genetic Heterogeneity of Usher Syndrome: Analysis of 151 Families with Usher Type I, Am. Kimberling, W.J., Moller, C.G., Davenport, S., et al., Linkage of Usher Syndrome Type I Gene ( USH1B) to the Long Arm of Chromosome 11, Genomics, 1992, no. Kaplan, J., Gerber, S., Bonneau, D., et al., A Gene for Usher Syndrome Type I ( USH1A) Maps to Chromosome 14q, Genomics, 1992, no. 431–444.Ĭremers, F.P.M., Kimberling, W.J., and Kulm, M., Development of a Genotyping Microarray for Usher Syndrome, J. ![]() 9–14.Īhmed, Z.M., Riazuddin, S., and Wilcox, E.R., The Molecular Genetics of Usher Syndrome, Clin. Markova, T.G., Nekrasova, N.V., Shagina, I.A., et al., Genetic Screening among the Children with Early Congenital Hearing Loss, Vestn. Pennings, R., Changing Horizons for People with Usher in the 21st Century: Clinical and Genetic Research in Usher Syndrome, in Genetic Research in Usher Syndrome, 2005, no. and Rohrschneider, K., Prevalence and Geographical Distribution of Usher Syndrome in Germany, Graefes Arch. Rosenberg, T., Haim, M., Hauch, A.M., et al., The Prevalence of Usher Syndrome and Other Retinal Dystrophy-Hearing Impairment Associations, Clin. Moller, C.G., Kimberling, W.J., Davenport, S.L., et al., Usher Syndrome: An Otoneurologic Study, Laryngoscope, 1989, no. 417–426.īoughman, J.A., Vernon, M., and Shaver, K.A., Usher Syndrome: Definition and Estimate of Prevalence from Two High-Risk Populations, J. Systemic Involvement and Age at Onset, Acta Ophthalmol. Haim, M., Prevalence of Retinitis Pigmentosa and Allied Disorders in Denmark: II. ![]() ![]() Marazita, M.L., Ploughman, L.M., Rawlings, B., et al., Genetic Epidemiological Studies of Early-Onset Deafness in the US School-Age Population, Am. Fortnum, H.M., Marshall, D.H., and Summerfield, A.Q., Epidemiology of the UK Population of Hearing-Impaired Children, Including Characteristics of Those with and without Cochlear Implants-Audiology, Aetiology, Comorbidity and Affluence, Int. ![]()
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