Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11

We evaluated linkage between the locus for multiple endocrine neoplasia type 1 (MEN1) and several polymorphic DNA markers on chromosome 11 in a single large pedigree. On the basis of the finding of a basic fibroblast growth factor (bFGF)-like substance circulating in plasma of MEN1 patients, we chos...

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Veröffentlicht in:Genomics (San Diego, Calif.) Calif.), 1989-04, Vol.4 (3), p.320-322
Hauptverfasser: Bale, Sherri J., Bale, Allen E., Stewart, Karen, Dachowski, Laura, McBride, O.W., Glaser, Tom, Green, Joseph E., Mulvihill, John J., Brandi, Maria Luisa, Sakaguchi, Kazushige, Aurbach, Gerald D., Marx, Stephen J.
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Sprache:eng
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Zusammenfassung:We evaluated linkage between the locus for multiple endocrine neoplasia type 1 (MEN1) and several polymorphic DNA markers on chromosome 11 in a single large pedigree. On the basis of the finding of a basic fibroblast growth factor (bFGF)-like substance circulating in plasma of MEN1 patients, we chose a bFGF-related gene known to be localized to 11q13 as one of the markers. This gene locus, INT2, was found to be closely linked to the MEN1 gene. Pairwise and multipoint analyses with INT2 confirm the recent finding by C. Larsson et al. (1988, Nature (London) 332: 85–87) of MEN1 linkage to another marker, skeletal muscle glycogen phosphorylase, at 11q13.
ISSN:0888-7543
1089-8646
DOI:10.1016/0888-7543(89)90336-4