Identical Twins and Chronic Myelocytic Leukemia
- 1 April 1965
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of internal medicine (1960)
- Vol. 115 (4) , 475-478
- https://doi.org/10.1001/archinte.1965.03860160101018
Abstract
I Introduction N RECENT years a number of reports describing an abnormal chromosome in patients with chronic myelocytic leukemia have appeared.1-10This abnormal chromosome appears to belong to the group of small acrocentric chromosomes and probably represents chromosome number 21. The chromosome has been named Ph1in relation to the city of Philadelphia where this abnormal chromosome was first described.3 The mechanism of production of this abnormal chromosome has been postulated to be either a deletion or translocation of the long arms of chromosome number 21. Since chromosome number 21 is small, it is easy to detect the deletion of the long arms of the chromosome morphologically; however, it has not been possible to detect whether the deleted parts have been translocated to other larger chromosomes or simply lost, since addition of such a small segment of chromosome has been impossible to observe with the present availableThis publication has 7 references indexed in Scilit:
- Cytogenetic Studies in Eosinophilic LeukemiaAnnals of Internal Medicine, 1965
- Specificity of the Philadelphia ChromosomeAnnals of Internal Medicine, 1964
- The Distribution of the Philadelphia Chromosome in Patients with Chronic Myelogenous LeukemiaBlood, 1963
- Chronic Granulocytic Leukemia and the Philadelphia ChromosomeBlood, 1963
- Comparison of Chromosome Constitution in Chronic Myelocytic Leukemia and Other Myeloproliferative DisordersBlood, 1962
- Chromosome Studies in Human Leukemia. II. Chronic Granulocytic LeukemiaJNCI Journal of the National Cancer Institute, 1961
- THE CHROMOSOME CONSTITUTION OF A HUMAN PHENOTYPIC INTERSEX1959