Abstract
Sequence-tagged sites (STSs) were developed for the human a-tropomyosin gene TPM4. One STS was used to amplify DNA from somatic cell hybrids to localize TPM4 to chromosome 19. The other, a product from a long-range PCR, was used directly as a probe to refine the localization of TPM4 to 19p13.1 by fluorescence in situ hybridization to metaphase chromosome spreads.
Original language | English |
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Pages (from-to) | 294-296 |
Journal | Cytogenetics and Cell Genetics |
Volume | 72 |
DOIs | |
Publication status | Published - 1996 |