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pubmed-article:2891602pubmed:abstractTextTwo single-copy DNA sequences, pG24E6.8 (D13S21) detecting a low-frequency MspI RFLP and pG14E1.9 (D13S22) detecting a high-frequency Dra I RFLP, have been isolated and cloned from a human chromosome 13-specific phage library and localized at 13q14. Their subband localization was described using a panel of cell lines from patients with different chromosome 13 deletions. A quantitative analysis of hybridization signals was carried out, taking for reference a single-copy DNA sequence from another chromosome. D13S21 and D13S22 were both assigned to q14.1-14.2, which also harbors the genes responsible for retinoblastoma and Wilson disease. The Dra I polymorphism detected by pG14E1.9 is a very suitable one for linkage studies in families with either disease.lld:pubmed
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pubmed-article:2891602pubmed:articleTitleLocalization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson disease.lld:pubmed
pubmed-article:2891602pubmed:affiliationDepartment of Human Genetics, State University of Groningen, The Netherlands.lld:pubmed
pubmed-article:2891602pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:2891602pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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