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A chromosomal abnormality (21q-) in primary thrombocytosis |
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| Authors: | P. Petit H. Van den Berghe |
| Affiliation: | (1) Centre de Diagnostic Hormonal, 196, Ch. d'Alsemberg, B-1180 Bruxelles, Belgium;(2) Division of Human Genetics, Department of Human Biology, University of Leuven, Minderbroedersstraat, 12, B-3000 Leuven, Belgium |
| Abstract: | Summary A patient with primary thrombocytosis was found to present an acquired deletion of the long arm of chromosome 21 (21q-). A similar observation reported in the literature is hereby confirmed. |
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