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Apparently changing patterns of inheritance in Alport's hereditary nephritis: Genetic heterogeneity versus altered diagnostic criteria

dc.contributor.authorEvans, Sarah Helenen_US
dc.contributor.authorErickson, Robert P.en_US
dc.contributor.authorKelsch, Roberten_US
dc.contributor.authorPeirce, John C.en_US
dc.date.accessioned2010-04-01T15:36:13Z
dc.date.available2010-04-01T15:36:13Z
dc.date.issued1980-04en_US
dc.identifier.citationEvans, Sarah Helen; Erickson, Robert P.; Kelsch, Robert; Peirce, John C. (1980). "Apparently changing patterns of inheritance in Alport's hereditary nephritis: Genetic heterogeneity versus altered diagnostic criteria." Clinical Genetics 17(4): 285-292. <http://hdl.handle.net/2027.42/66090>en_US
dc.identifier.issn0009-9163en_US
dc.identifier.issn1399-0004en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/66090
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7371220&dopt=citationen_US
dc.format.extent575000 bytes
dc.format.extent3110 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.rights1980 Blackwell Munksgaarden_US
dc.subject.otherAlport's Syndromeen_US
dc.subject.otherDominant Inheritanceen_US
dc.subject.otherGenetic Heterogeneityen_US
dc.subject.otherNephritisen_US
dc.subject.otherSegregation Ratiosen_US
dc.subject.otherX-linkageen_US
dc.titleApparently changing patterns of inheritance in Alport's hereditary nephritis: Genetic heterogeneity versus altered diagnostic criteriaen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Human Genetics, Michigan, USAen_US
dc.contributor.affiliationumDepartments of Pediatrics, University of Michigan School of Medicine, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumNephrology Department, St. Mary's Hospital, Grand Rapids, Michigan, USAen_US
dc.identifier.pmid7371220en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/66090/1/j.1399-0004.1980.tb00149.x.pdf
dc.identifier.doi10.1111/j.1399-0004.1980.tb00149.xen_US
dc.identifier.sourceClinical Geneticsen_US
dc.identifier.citedreferenceAlport, A. C. ( 1927 ). Hereditary familial congenital haemorrhagic nephritis. Brit. med. J. 1, 504 – 506.en_US
dc.identifier.citedreferenceArnott, E. J., M. d'A. Crawfurd & P. J. Tog-nill ( 1966 ). Anterior lenticonus and Alport's syndrome. Brit. J. Ophthal. 50, 390 – 403.en_US
dc.identifier.citedreferenceBen-Ishay, D., S. Biran & T. D. Ullmann ( 1967 ). Familial nephritis. Israel J. med. Sci. 3, 106 – 112.en_US
dc.identifier.citedreferenceChavis, R. M. & T. Groshong ( 1973 ). Corneal arcus in Alport's syndrome. Amer. J. Ophthal. 75, 793 – 794.en_US
dc.identifier.citedreferenceChen, A. T. L. & A. Falek ( 1969 ). Centrameres in human meiotic chromosomes. Science 166, 1008 – 1010.en_US
dc.identifier.citedreferenceCohen, M. M., G. Cassady & B. L. Hanna ( 1961 ). A genetic study of hereditary renal dysfunction with associated nerve deafness. Amer. J. hum. Genet. 13, 379 – 389.en_US
dc.identifier.citedreferenceDzubia, P., A. Kobierska-Szczcpanska & K. Jonczyk ( 1975 ). Genetical investigations of familial nephropathy. Gen. Pol. 16, 229 – 233.en_US
dc.identifier.citedreferenceFerguson, A. C. & C. P. Rance ( 1972 ). Hereditary nephropathy with nerve deafness (Alport's syndrome). Amer. J. Dis. Child. 124, 83 – 88.en_US
dc.identifier.citedreferenceGaboardi, F., A. Edefonti, E. Imbasciata, A. Tarantino, M. J. Mihatsch & H. U. Zollinger ( 1974 ). Alport's syndrome (progressive hereditary nephritis). Clin. Neph. 2, 143 – 156.en_US
dc.identifier.citedreferenceGraham, J. B. ( 1959 ). Hereditary chronic kidney disease: An alternative to partial sex-linkage in the Utah kindred. Amer. J. hum. Genet. 11, 333 – 338.en_US
dc.identifier.citedreferenceHallberg, A. ( 1976 ). Alport's syndrome. Acta paediat. scand. 65, 49 – 56.en_US
dc.identifier.citedreferenceIversen, U. M. ( 1974 ). Hereditary nephropathy with hearing loss “Alport's syndrome”. Acta paediat. scand. Suppl. 245, 5 – 23.en_US
dc.identifier.citedreferenceJacobs, P. A. & A. Ross ( 1966 ). Structural abnormalities of the Y-chromosome in man. Nature 210, 352 – 354.en_US
dc.identifier.citedreferenceMacNeill, E. & R. F. Shaw ( 1973 ). Segregation ratios in Alport's syndrome. J. med. Genet. 10, 23 – 26.en_US
dc.identifier.citedreferenceO'Neill, W. M., C. L. Atkin & H. A. Bloomer ( 1978 ). Hereditary nephritis. A re-exarnination of its clinical and genetic features. Ann. int. Med. 88, 176 – 182.en_US
dc.identifier.citedreferencePearson, P. L. & M. Bobrow ( 1970 ). Definitive evidence for the short arm of the Y-chromosome associating with the X-chromosome during meiosis in the human male. Nature 226, 959 – 961.en_US
dc.identifier.citedreferencePerkoff, G. T., F. E. Stephens, D. A. Dolowitz & F. H. Tyler ( 1951 ). A clinical study of hereditary interstitial pyelonephritis. AMA Arch. int. Med. 88, 191 – 200.en_US
dc.identifier.citedreferencePreus, M. & F. C. Fraser ( 1971 ). Genetics of hereditary nephropathy with deafness (AIport's disease). Clin. Genet. 2, 331 – 337.en_US
dc.identifier.citedreferencePurriel, P., M. Drets, E. Pascale, R. S. Cestau, A. Borras, W. A. Ferreira, A. de Lucca & L. Fernandez ( 1970 ). Familial hereditary nephropathy (Alport's syndrome). Amer. J. Med. 49, 753 – 773.en_US
dc.identifier.citedreferenceRoyer, P., R. Habib, H. Mathieu & M. Broyer ( 1974 ). Pediatric Nephrology. Philadelphia, W. B. Saunders, pp. 37 – 42.en_US
dc.identifier.citedreferenceShaw, R. F. & R. A. Glover ( 1961 ). Abnormal segregation in hereditary renal disease with deafness. Amer. J. hum. Genet, 13, 89 – 97.en_US
dc.identifier.citedreferenceShaw, F. F. & R. J. Kallen ( 1976 ). Population genetics of Alport's syndrome. Nephron 16, 427 – 432.en_US
dc.identifier.citedreferenceTeisberg, P., K. A. GrÖttum, E. Myhre & A. Flatmark ( 1973 ). In vivo activation of complement in hereditary nephropathy. Lancet ii, 356 – 358.en_US
dc.identifier.citedreferenceTishler, P. V. & B. Rosner ( 1974 ). The genetics of the Alport syndrome. Birth Defects 10, 93 – 99.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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