Abstract
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.
Lingua originale | Inglese |
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pagine (da-a) | 199-202 |
Numero di pagine | 4 |
Rivista | Molecular and Cellular Probes |
Volume | 13 |
Numero di pubblicazione | 3 |
DOI | |
Stato di pubblicazione | Pubblicato - giu 1999 |
Pubblicato esternamente | Sì |