Chromosomal evidence of a common stem cell in acute lymphoblastic leukemia and chronic granulocytic leukemia.
dc.contributor.author | Harrison, Christine J | |
dc.contributor.author | Chang, James | |
dc.contributor.author | Johnson, Deborah | |
dc.contributor.author | Jack, E | |
dc.contributor.author | Scott, David | |
dc.contributor.author | Harris, R | |
dc.date.accessioned | 2011-03-12T23:59:40Z | |
dc.date.available | 2011-03-12T23:59:40Z | |
dc.date.issued | 1984-12 | |
dc.identifier.citation | Chromosomal evidence of a common stem cell in acute lymphoblastic leukemia and chronic granulocytic leukemia. 1984, 13 (4):331-6 Cancer Genet. Cytogenet. | en |
dc.identifier.issn | 0165-4608 | |
dc.identifier.pmid | 6595053 | |
dc.identifier.doi | 10.1016/0165-4608(84)90076-1 | |
dc.identifier.uri | http://hdl.handle.net/10541/124422 | |
dc.description.abstract | A patient with acute lymphoblastic leukemia (ALL) was found, at the time of diagnosis, to have an unusual Philadelphia chromosome (Ph1) with a satellite marker. The disease evolved into the chronic phase of chronic granulocytic leukemia (CGL), with persistance of the marker. Two months later, the patient died of ALL. | |
dc.language.iso | en | en |
dc.subject.mesh | Adult | |
dc.subject.mesh | Chromosome Aberrations | |
dc.subject.mesh | Chromosome Disorders | |
dc.subject.mesh | Chromosomes, Human, 21-22 and Y | |
dc.subject.mesh | Chromosomes, Human, 6-12 and X | |
dc.subject.mesh | Female | |
dc.subject.mesh | Hematopoietic Stem Cells | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Karyotyping | |
dc.subject.mesh | Leukemia, Lymphoid | |
dc.subject.mesh | Leukemia, Myeloid | |
dc.subject.mesh | Metaphase | |
dc.title | Chromosomal evidence of a common stem cell in acute lymphoblastic leukemia and chronic granulocytic leukemia. | en |
dc.type | Article | en |
dc.contributor.department | Paterson Laboratories and Radiotherapy Department, CHristie Hospital and Holt Radium Institute, Manchester M20 9BX | en |
dc.identifier.journal | Cancer Genetics and Cytogenetics | en |
html.description.abstract | A patient with acute lymphoblastic leukemia (ALL) was found, at the time of diagnosis, to have an unusual Philadelphia chromosome (Ph1) with a satellite marker. The disease evolved into the chronic phase of chronic granulocytic leukemia (CGL), with persistance of the marker. Two months later, the patient died of ALL. |