Genesis of the Philadelphia chromosome: Possible points of breakage in chromosome No. 22
- 12 February 2009
- journal article
- Published by Springer Nature in Hereditas
- Vol. 79 (2) , 301-303
- https://doi.org/10.1111/j.1601-5223.1975.tb01487.x
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- A New Consistent Chromosomal Abnormality in Chronic Myelogenous Leukaemia identified by Quinacrine Fluorescence and Giemsa StainingNature, 1973
- Banding in Human Chromosomes treated with TrypsinNature New Biology, 1972
- Distinguishing between the Chromosomes involved in Down's Syndrome (Trisomy 21) and Chronic Myeloid Leukaemia (Ph1) by FluorescenceNature, 1971
- Identification of the Philadelphia chromosome as a number 22 by quinacrine mustard fluorescence analysisExperimental Cell Research, 1970
- NOMENCLATURE FOR CENTROMERIC POSITION ON CHROMOSOMESHereditas, 1964