Prenatal diagnosis of hemoglobin opathies and other hematologic diseases
- 1 October 1979
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 95 (4), 501-513
- https://doi.org/10.1016/s0022-3476(79)80753-2
Abstract
No abstract availableThis publication has 36 references indexed in Scilit:
- The molecular basis of α-thalassemias: Frequent occurrence of dysfunctional α loci among non-Asians with Hb H diseaseCell, 1979
- Sickle-Cell Anemia: Molecular and Cellular Bases of Therapeutic ApproachesNew England Journal of Medicine, 1978
- Sickle-Cell Anemia: Molecular and Cellular Bases of Therapeutic ApproachesNew England Journal of Medicine, 1978
- Sickle-Cell Anemia: Molecular and Cellular Bases of Therapeutic ApproachesNew England Journal of Medicine, 1978
- Erythrocytic mechanism of sickle cell resistance to malaria.Proceedings of the National Academy of Sciences, 1978
- Identification of a Nondeletion Defect in α-ThalassemiaNew England Journal of Medicine, 1977
- Continuous Subcutaneous Administration of Deferoxamine in Patients with Iron OverloadNew England Journal of Medicine, 1977
- Gene deletion as the cause of α thalassaemia: Genetic lesion in homozygous α thalassaemia (hydrops fetalis)Nature, 1974
- ALPHA‐ AND BETA‐THALASSEMIA IN THAILAND*Annals of the New York Academy of Sciences, 1969
- Human Embryonic HemoglobinsCold Spring Harbor Symposia on Quantitative Biology, 1964