A Swedish Family with Haemolytic Anaemia, Heinz Bodies and an Abnormal Haemoglobin
- 1 August 1967
- journal article
- research article
- Published by Wiley in Scandinavian Journal of Haematology
- Vol. 4 (4) , 241-248
- https://doi.org/10.1111/j.1600-0609.1967.tb01625.x
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Haemoglobin Köln (β–98 Valine → Methionine): An Unstable Protein Causing Inclusion-Body AnaemiaNature, 1966
- Erythrocyte Metabolism in HemolysisNew England Journal of Medicine, 1965
- Familial Haemolytic Anaemia with Erythrocyte Inclusion Bodies, Bilifuscinuria and Abnormal Haemoglobin (Haemoglobin Galliera Genova)British Journal of Haematology, 1965
- Human HaemoglobinsJournal of Medical Genetics, 1965
- Hereditary Heinz-body Anaemia, Thrombocyttopenia, and Haemoglobinopathy (Hb Koln) in a Glasgow FamilyBMJ, 1964
- Hereditary Heinz‐Body AnaemiaBritish Journal of Haematology, 1964
- Congenital Heinz‐Body AnaemiaBritish Journal of Haematology, 1964
- Haemoglobin Bart’s and H in a Swedish BoyActa Haematologica, 1964
- Studies on an Abnormal Hemoglobin Causing Hereditary Congenital CyanosisActa Paediatrica, 1960
- Haemoglobin H and Inclusion‐Body Anaemia in a Swedish FamilyActa Paediatrica, 1958