Prenatal diagnosis of hemoglobin H disease
- 1 February 1978
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 92 (2), 278-281
- https://doi.org/10.1016/s0022-3476(78)80025-0
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
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- Prenatal Diagnosis of α-ThalassemiaNew England Journal of Medicine, 1976
- Midtrimester Amniocentesis for Prenatal DiagnosisJAMA, 1976
- Alpha thalassemia in American-born Filipino infantsThe Journal of Pediatrics, 1975
- Deletion of α-globin genes in haemoglobin-H disease demonstrates multiple α-globin structural lociNature, 1975
- Gene deletion as the cause of α thalassaemia: Genetic lesion in homozygous α thalassaemia (hydrops fetalis)Nature, 1974
- Gene deletion as the cause of α thalassaemia: The severe form of α thalassaemia is caused by a haemoglobin gene deletionNature, 1974
- ALPHA‐ AND BETA‐THALASSEMIA IN THAILAND*Annals of the New York Academy of Sciences, 1969
- An Improved Method for the Characterization of Human Haemoglobin Mutants: Identification of α2β295GLU, Haemoglobin N (Baltimore)Nature, 1965
- Alpha-chain Thalassemia and Hydrops Fetalis in Malaya: Report of Five CasesBlood, 1962