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. 2000 Jan;66(1):326-30.
doi: 10.1086/302718.

A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23

Y A Lee, H P Stevens, E Delaporte, U Wahn, A Reis

A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23

Y A Lee et al. Am J Hum Genet. 2000 Jan.
No abstract available

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Figures

Figure 1
Figure 1
Pedigrees of families A and B with Huriez syndrome. Affected family members are denoted by blackened symbols. The most likely haplotype for seven markers from an 8-cM interval between D4S1544 and D4S2966 is shown below each individual.
Figure 2
Figure 2
Linkage map of microsatellite markers from chromosome 4q23. Genetic distances are indicated in centimorgans. Markers are arranged in map order according to the final Généthon human linkage map (Dib et al. 1996). In the candidate region, markers are ordered according to their score on the TNG radiation hybrid panel. Here, relative positions are noted in cR after assigning 0 cR to marker D4S1544. The wild-type allele is represented by a white bar, the mutated allele by a gray bar. In the candidate region, markers IBS are noted in boldface type. The recombination events in members 4.11 and 6.1 of family 1 and 2.5 of family 2 are shown. The minimal candidate region for Huriez syndrome is marked. “aff.” indicates affected; “not aff.,” not affected.
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References

Electronic-Database Information

    1. Généthon, http://www.genethon.fr/
    1. Human Gene Map, The, http://www.ncbi.nlm.nih.gov/SCIENCE96/
    1. Online Mendelian Inheritance in Man (OMIM), http://www.ncbi.nlm.nih.gov/Omim (for Huriez syndrome [MIM 181600])

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