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Title: Genetics of classic Alport's syndrome. Author: Flinter FA, Cameron JS, Chantler C, Houston I, Bobrow M. Journal: Lancet; 1988 Oct 29; 2(8618):1005-7. PubMed ID: 2902439. Abstract: 41 families with classic Alport's syndrome (hereditary nephritis with sensorineural deafness) were studied. All their pedigrees were compatible with X-linked inheritance. DNA probes were used to investigate genetic linkage in these families. Linkage to probe S21 (DXS17) was confirmed (LOD score = 4.72 at 0 = 0.06), localising the gene for Alport's syndrome to the middle of Xq; thus the disorder is X-chromosomal in nature.[Abstract] [Full Text] [Related] [New Search]