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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/7168
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dc.contributor.authorHunt, C.-
dc.contributor.authorEyre, H.-
dc.contributor.authorAkkari, P.-
dc.contributor.authorMeredith, C.-
dc.contributor.authorDorosz, S.-
dc.contributor.authorWilton, S.-
dc.contributor.authorCallen, D.-
dc.contributor.authorLaing, N.-
dc.contributor.authorBaker, E.-
dc.date.issued1995-
dc.identifier.citationCytogenetic and Genome Research, 1995; 71(1):94-95-
dc.identifier.issn0301-0171-
dc.identifier.issn1424-859X-
dc.identifier.urihttp://hdl.handle.net/2440/7168-
dc.description.abstractA sequence tagged site (STS) was developed for the human beta tropomyosin gene (TPM2). The STS was used to amplify DNA from somatic cell hybrids to localise TPM2 to human chromosome 9. Genomic clones isolated with the STS product were in turn used in fluorescence in situ hybridisation to metaphase chromosome spreads to further localise TPM2 to 9p13.-
dc.description.statementofresponsibilityHunt, C C ; Eyre, H J ; Akkari, P A ; Meredith, C ; Dorosz, S M ; Wilton, S D ; Callen, D F ; Laing, N G ; Baker, E-
dc.language.isoen-
dc.publisherS. Karger-
dc.source.urihttp://dx.doi.org/10.1159/000134070-
dc.subjectHybrid Cells-
dc.subjectChromosomes, Human, Pair 9-
dc.subjectAnimals-
dc.subjectHumans-
dc.subjectMice-
dc.subjectTropomyosin-
dc.subjectDNA Primers-
dc.subjectIn Situ Hybridization, Fluorescence-
dc.subjectChromosome Mapping-
dc.subjectBase Sequence-
dc.subjectSequence Tagged Sites-
dc.subjectMolecular Sequence Data-
dc.subjectMale-
dc.titleAssignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation-
dc.typeJournal article-
dc.identifier.doi10.1159/000134070-
pubs.publication-statusPublished-
dc.identifier.orcidCallen, D. [0000-0002-6189-9991]-
Appears in Collections:Aurora harvest 5
Paediatrics publications

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