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American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1993 Jul;53(1):71–79.

Genetic heterogeneity in families with hereditary multiple exostoses

April Cook, Wendy Raskind, Susan Halloran Blanton, Richard M Pauli, Ronald G Gregg, Claire A Francomano, Eric Puffenberger, Ernest U Conrad, Gregory Schmale, Gerard Schellenberg, Ellen Wijsman, Jacqueline T Hecht, Dan Wells, Michael J Wagner
PMCID: PMC1682231  PMID: 8317501

Abstract

We have carried out a linkage analysis on 11 families segregating gene(s) for hereditary multiple exostoses (EXT). Four highly informative, short tandem-repeat (STR) markers that have been physically mapped to an interval surrounding the Langer-Giedion chromosomal region (8q24.11-q24.13) were used in a multipoint linkage analysis. Significant evidence for linkage of EXT with genetic heterogeneity was found. A model of heterogeneity with linkage of the disease gene to the STR markers in 70% of the families (with a 95% confidence interval of 26%–96%) produced a maximum LOD score of 8.11, with the most likely position of EXT between D8S85 and D8S199. Thus there are at least two genes that are capable of causing hereditary multiple exostoses, one in the Langer-Giedion region and one at another, unlinked location.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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