Autosomal dominant branchio-oto-renal syndrome--localization of a disease gene to chromosome 8q by linkage in a Dutch family

Branchio-oto-renal syndrome (BOR) is an autosomal dominant disorder with variable clinical manifestations affecting branchial, renal and auditory development. Varying clinical expression of the disease between different families suggests that multiple loci may be involved. However, the possibility of genetic heterogeneity as the cause of clinical variability cannot be resolved until the gene(s) causing BOR syndrome are mapped. DNA from four generations of a family with autosomal dominant BOR syndrome have been typed with a series of genetic markers on the long arm of chromosome 8. Using two po... Mehr ...

Verfasser: Kumar, Shrawan
Kimberling, William J.
Kenyon, Judy B.
Smith, Richard J. H.
Marres, Henri A. M.
Cremers, Cor W. R. J.
Dokumenttyp: TEXT
Erscheinungsdatum: 1992
Verlag/Hrsg.: Oxford University Press
Schlagwörter: ORIGINAL ARTICLES
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-28992295
Datenquelle: BASE; Originalkatalog
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Link(s) : http://hmg.oxfordjournals.org/cgi/content/short/1/7/491