Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12–q13
Takahashi, M. ; Rapley, E. ; Biggs, P.J. ; Lakhani, S.R ; Cooke, D. ; Hansen, J. ; Blair, E. ; Hofmann, B. ; Siebert, R. ; Turner, G. ; Evans, D.G. ; Schrander-Stumpel, C. ; Beemer, F.A. ; van Vloten, W.A. ; Breuning, M.H. ; van den Ouweland, A. ; Halley, D. ; Delpech, B. ; Cleveland, M. ; Leigh, I. ; Chapman, P. ; Burn, J. ; Hohl, D. ; Görög, J.-P. ; Seal, S.
Springer
Published 2000
Springer
Published 2000
| ISSN: |
1432-1203
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|---|---|
| Source: |
Springer Online Journal Archives 1860-2000
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| Topics: |
Biology
Medicine
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| Notes: |
Abstract. Familial cylindromatosis is an autosomal dominant predisposition to multiple neoplasms of the skin appendages. The susceptibility gene has previously been mapped to chromosome 16q12–q13 and has features of a recessive oncogene/tumour suppressor gene. We have now evaluated 19 families with this disease by a combination of genetic linkage analysis and loss of heterozygosity in cylindromas from affected individuals. All 15 informative families show linkage to this locus, providing no evidence for genetic heterogeneity. Recombinant mapping has placed the gene in an interval of approximately 1 Mb. There is no evidence, between families, of haplotype sharing that might be indicative of common founder mutations.
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| Type of Medium: |
Electronic Resource
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| URL: |