Diagnosls of α thalassemia in the newborn. cord blood survey utilizing gene mapping
Author:
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine
Reference18 articles.
1. Localisation of the human α-globin structural gene to chromosome 16 in somatic cell hybrids by molecular hybridisation;Deisseroth;Cell,1977
2. Regional assignment of genes for human α globin and phosphoglycollate phosphatase to the short arm of chromosome 16;Koeffler;Proc Natl Acad Sci USA,1981
3. α-and beta thalassemia in Thailand;Wasi;Ann NY Acad Sci,1969
4. The thalassaemia syndromes;Weatherall,1981
5. The molecular basis of α-thalassemias: Frequent occurrence of dysfunctional a loci among non-Asians with HbH disease;Orkin;Cell,1979
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Haemoglobin Manukau β67[E11] Val→Gly: transfusion-dependent haemolytic anaemia ameliorated by coexisting alpha thalassaemia;British Journal of Haematology;1993-10
2. Congenital Anemias in Macau;Hemoglobin;1988-01
3. The state of the art of clinical gene diagnosis;Journal of Clinical Laboratory Analysis;1987
4. Hemoglobinopathies in Southeast Asia;Hemoglobin;1987-01
5. Functional Activity of the Triplicated ααα4.2/ Gene Rearrangement;Hemoglobin;1986-01
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