... and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. 2022 Myeloproliferative neoplasms Hematologic malignancies Genetics Eosinophilia Polycythemia vera (PV...

... with Thalassaemia Trait E va Raik, E lizabeth Powell and Susan G ordon Haematology Department, Kanematsu Memorial Institute, Sydney Hospital, Sydney Key Words. Anglo-Saxon family Genetics Heterogeneity of /i-thalassaemia Inheritance of ^-thalassaemia Thalassaemia Abstract. Study of a large Anglo-Saxon...

... of the danger that mating between a carrier of this thalassaemia and a carrier of classical β -thalassaemia could result in the birth of children with Cooley’s disease. Thalassaemia Haemoglobin pattern Genetics Biosynthetic studies 27 04 1977 28 10 1977 3 3 2009 © 1978 S. Karger...

... in the May-Grünwald Giemsa procedure and is similar, therefore, to the eosinophil peroxidase. In the phenotype observed, 2 genetic changes are probably involved: one is a change in the regulation of NPNL granulation, the other is a mutation in the myeloperoxidase structural gene. In the light of these new...

... or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Epistasis Genetics Linkage Sickle mutations Sickle Cell Disease Haemoglobin. Proc. Int. Meeting, London 1986 Acta haemat. 78: 184-185(1987) Genetic Heterogeneity of Sickle...

...B. Presentey The structure of human eosinophils genetically lacking peroxidase is described. Structural changes were discerned in the specific granules of the deficient eosinophils as compared to normal eosinophils. Apart from the inhibition of peroxidase formation, this mutation also affects...