Types of α-Globin Gene Deficiencies in Chinese Newborn Babies in the Guangxi Region, P.R. China
- 1 January 1992
- journal article
- Published by Taylor & Francis in Hemoglobin
- Vol. 16 (4) , 325-328
- https://doi.org/10.3109/03630269208998877
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Hb Hekinan Observed in Three Chinese from Macau; Identification of the Gag→Gat Mutation in the αl-Globin GeneHemoglobin, 1990
- A review of the molecular genetics of the human alpha-globin gene clusterBlood, 1989
- The Types and Distribution of α-Thalassemia-2 in ChinaHemoglobin, 1988
- The Incidence of α-Thalassemia in South ChinaHemoglobin, 1988
- Two different quadruplicated α globin gene arrangementsBritish Journal of Haematology, 1987
- The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genesBlood, 1984
- Globin structural mutant α125Leu→Pro is a novel cause of α-thalassaemiaNature, 1982
- Construction of Human Gene Libraries from Small Amounts cf Peripheral Blood: Analysis of β-Like Globin GenesHemoglobin, 1981
- HÆMOGLOBIN-H DISEASE DUE TO A UNIQUE HÆMOGLOBIN VARIANT WITH AN ELONGATED α-CHAINThe Lancet, 1971