+ Site Statistics
+ Search Articles
+ PDF Full Text Service
How our service works
Request PDF Full Text
+ Follow Us
Follow on Facebook
Follow on Twitter
Follow on LinkedIn
+ Subscribe to Site Feeds
Most Shared
PDF Full Text
+ Translate
+ Recently Requested

Compound Heterozygosity For Triplicated a-Globin Gene and ( SEA) a-Globin Gene Deletion: Implication For Thalassaemia Screening



Compound Heterozygosity For Triplicated a-Globin Gene and ( SEA) a-Globin Gene Deletion: Implication For Thalassaemia Screening



British Journal of Haematology 110(2): 493-499




Please choose payment method:






(PDF emailed within 0-6 h: $19.90)

Accession: 062871580

Download citation: RISBibTeXText

DOI: 10.1046/j.1365-2141.2000.02165-1.x


Related references

Compound heterozygosity for triplicated alpha-globin gene and (- -(SEA)) alpha-globin gene deletion: implication for thalassaemia screening. British Journal of Haematology 110(2): 498-499, 2000

Thalassemia Intermedia And Extramedullary Hematopoiesis Associated With Compound Heterozygosity For The 532 Bp Deletion Of The -Globin Gene And Gene Deletion Hereditary Persistence Of Fetal Hemoglobin. Hemoglobin 25(1): 91-96, 2001

Thalassemia intermedia and extramedullary hematopoiesis associated with compound heterozygosity for the 532 bp deletion of the beta-globin gene and gene deletion hereditary persistence of fetal hemoglobin. Hemoglobin 25(1): 91-96, 2001

Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb beta-globin gene deletion. European Journal of Haematology 78(1): 82-85, 2007

A 13-bp deletion in the 3' untranslated region of the β-globin gene causes β-thalassemia major in compound heterozygosity with IVSII-1 mutation. Medical Principles and Practice 20(5): 488-490, 2011

Haematological phenotypes in a family with triplicated alpha-globin gene, beta zero 39 and delta+27 thalassaemia mutations. Clinical and Laboratory Haematology 14(4): 289-292, 1992

Severe thalassaemia intermedia caused by interaction of homozygosity for alpha-globin gene triplication with heterozygosity for beta zero-thalassaemia. British Journal of Haematology 86(2): 377-379, 1994

Compound heterozygosity for a rare small deletion and a common point mutation in the beta-globin gene: report of two Chinese families. International Journal of Laboratory Hematology 33(1): 79-84, 2011

The triplicated alpha-globin gene locus in beta-thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies. British Journal of Haematology 95(3): 467-471, 1996

Interaction of triplicated alpha-globin genes and beta-globin gene mutations. Blood 86(10 Suppl. 1): 484A, 1995

Beta-thalassemia intermedia due to compound heterozygosity for two beta-globin gene promoter mutations, including a novel TATA box deletion. Pediatric Blood and Cancer 50(2): 363-366, 2008

A genetic combination of silent beta-thalassaemia, high Hb A2 beta-thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermedia. Journal of Medical Genetics 21(2): 153-156, 1984

Novel point mutation of the α2-globin gene (HBA2) and a rare 2.4 kb deletion of the α1-globin gene (HBA1), identified in two chinese patients with Hb H disease. Hemoglobin 38(3): 213-215, 2014

Identification of the linkage of a 1.357 KB beta-globin gene deletion and A gamma-globin gene triplication in a Chinese family. Hemoglobin 34(4): 343-353, 2010

Inactivation of human a-globin gene expression by a de novo deletion located upstream of the a-globin gene cluster. Proceedings of the National Academy of Sciences of the United States of America 87(23): 31-5, 1990