THALASSÆMIA AS A MODEL OF RECESSIVE GENETIC DISEASE IN THE COMMUNITY
- 1 September 1980
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 316 (8194), 574-578
- https://doi.org/10.1016/s0140-6736(80)92003-6
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Effect of introducing antenatal diagnosis on reproductive behaviour of families at risk for thalassaemia major.BMJ, 1980
- DEVELOPMENT OF A QUANTITATIVE IMMUNOASSAY FOR THE CYSTIC FIBROSIS GENEThe Lancet, 1980
- Prenatal diagnosis of hemoglobin opathies and other hematologic diseasesThe Journal of Pediatrics, 1979
- Prenatal Diagnosis of HemoglobinopathiesNew England Journal of Medicine, 1976
- COMPREHENSIVE TESTING FOR THALASSEMIA TRAITAnnals of the New York Academy of Sciences, 1974
- Thalassaemia in the BritishBMJ, 1973
- Incidence of -Thalassaemia Trait among Cypriots in LondonBMJ, 1972
- Incidence of fibrocystic disease in Wessex.Journal of Medical Genetics, 1968
- Abnormal human haemoglobins: Separation and characterization of the α and β chains by chromatography, and the determination of two new variants, Hb chesapeake and Hb J (Bangkok)Journal of Molecular Biology, 1966