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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR.

The recently isolated human WHN gene has been previously assigned to chromosome 17q11-12 using radiation hybrids. In this study, we constructed a YAC contig covering 17q11.2 between crystallinBA1 and neurofibromatosis 1 genes. By ordering known and novel markers, we determined the position of the WHN gene, and of the closely linked retinal 4 and sodium/dicarboxylate cotransporter genes. We also identified a new mononucleotide polymorphism contained within the untranslated exon 1 of the WHN gene, which may be useful for linkage and LOH studies.[1]

References

  1. Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR. Corrado, L., Colapietro, P., Larizza, L., Riva, P. Mol. Cell. Probes (1999) [Pubmed]
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