Brief Report: Chromosome-21 and Paroxysmal Nocturnal Hemoglobinuria
Open Access
- 1 August 1964
- journal article
- research article
- Published by American Society of Hematology in Blood
- Vol. 24 (2) , 160-163
- https://doi.org/10.1182/blood.v24.2.160.160
Abstract
No strong morphologic or biochemical support was found for the concept that paroxysmal nocturnal hemoglobinuria was due to a chromosomal deletion.This publication has 5 references indexed in Scilit:
- Studies of Leukocyte Alkaline Phosphatase in Mongolism: A Possible Chromosome MarkerBlood, 1963
- A Comparison of Leukocyte Alkaline Phosphatase Determinations in 200 Patients with Mongolism and in 200 Familial ControlsNew England Journal of Medicine, 1963
- Études chromosomiques dans quelques anémies hémolytiquesActa Haematologica, 1962
- THE ERYTHROCYTE ACETYLCHOLINESTERASE ENZYME IN PAROXYSMAL NOCTURNAL HEMOGLOBINURIA1960
- A STUDY OF CHOLINESTERASE ACTIVITY IN THE BLOOD OF PATIENTS WITH HEMATOLOGIC DISEASE1949