Restriction fragment length polymorphism caused by a deletion within the human c-abl gene (ABL).
A restriction fragment length polymorphism at the human c-abl locus (ABL) has been detected in 67 unrelated individuals by agarose gel electrophoresis and Southern blot hybridization using 32P-labeled v-abl probes. This polymorphism is generated by the existence of two alleles, a and b, which are in...
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| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
1986
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC323532/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3010299/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.83.10.3447 |
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