Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region |
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Authors: | Tiina Alitalo Torben A. Kruse Peter Ahrens Hans M. Albertsen Aldur W. Eriksson Albert de la Chapelle |
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Affiliation: | (1) Department of Medical Genetics, University of Helsinki, Haartmaninkatu 3, SF-00290 Helsinki, Finland;(2) Folkhälsan Institute of Genetics, Helsinki, Finland;(3) Institute of Human Genetics, University of Aarhus, Aarhus, Denmark;(4) Institute of Human Genetics, Free University, Amsterdam, The Netherlands;(5) Department of Medical Genetics, University of Helsinki, Haartmaninkatu 3, SF-00290 Helsinki, Finland |
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Abstract: | Summary To provide a more precise genetic map of the p22.3–p21.2 region on the short arm of the human X chromosome, we performed multilocus linkage studies in an expanded database including 31 retinoschisis families and 40 normal families. Twelve loci from this region were examined. Although significant lod scores were observed between various pairs of markers by two-point linkage analysis, the confidence limits were found to be broad. The most likely gene order on the basis of multilocus analysis was Xpter-DXS89-DXS85-DXS16-(DXS207, DXS43)-DXS274-(DXS41, DXS92)-ZFX-DXS164-Xcen. All other alternative orders were excluded by odds of at least 401. |
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