+ Site Statistics
References:
54,258,434
Abstracts:
29,560,870
PMIDs:
28,072,757
+ 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 hemoglobin E-Saskatoon and ß-thalassemia



Compound heterozygosity for hemoglobin E-Saskatoon and ß-thalassemia



Journal of Obstetrics and Gynaecology Research 36(5): 1148




Please choose payment method:






(PDF emailed within 1 workday: $29.90)

Accession: 052269083

Download citation: RISBibTeXText

PMID: 21058451


Related references

Compound Heterozygosity for Hb E-Saskatoon and -Thalassemia. Hemoglobin 15(4): 345-346, 1991

Compound heterozygosity for Hb E-Saskatoon and beta-thalassemia. Hemoglobin 15(4): 345-346, 1991

Compound Heterozygosity for Hb E-Saskatoon or 2 2 22(B4)GluLys and -Thalassemia Type Ivs-I-6 (TC). Hemoglobin 14(4): 449-451, 1990

Thalassemia intermedia in HbH-CS disease with compound heterozygosity for β-thalassemia: Challenges in hemoglobin analysis and clinical diagnosis. Genes & Genetic Systems 84(1): 67-71, 2009

Thalassemia intermedia in HbH-CS disease with compound heterozygosity for beta-thalassemia: challenges in hemoglobin analysis and clinical diagnosis. Genes and Genetic Systems 84(1): 67-71, 2009

Compound heterozygosity for unstable hemoglobin Genova and beta(o)-thalassemia associated with early onset of thalassemia major syndrome. Haematologica 90(1): Ecr04, 2005

Compound heterozygosity for the 532-BP deletion beta thalassemia and hereditary persistence of fetal hemoglobin -2 associated with thalassemia intermedia and extramedullary hematopoiesis. Blood 94(10 SUPPL 1 PART 2): 35b, Nov 15, 1999

Compound heterozygosity for Hb E-Saskatoon or alpha 2 beta 2(22)(B4)Glu----Lys and beta-thalassemia type IVS-I-6 (T----C). Hemoglobin 14(4): 449-451, 1990

Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia. American Journal of Hematology 83(9): 760, 2008

Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India. Hemoglobin 42(2): 84-90, 2018

A Severe Case of Hemoglobin H Disease due to Compound Heterozygosity for Deletion of the Major α-Globin Regulatory Element (MCS-R2) and α0-Thalassemia. Acta Haematologica 138(1): 61-64, 2017

Frequency of hemoglobin E/β-thalassemia compound heterozygotes with low hemoglobin F phenotype among cases with a diagnosis of hemoglobin E homozygote, determined by high-performance liquid chromatography, in prenatal control program for β-thalassemia. Annals of Hematology 96(10): 1763-1765, 2017

Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and β-thalassemia or Hb Sabine confirms the functional role of the Aγ ˆ’ 158 C T m. 2008

The first case of a compound heterozygosity for Hb E-Saskatoon and HbS. Haematologica 88(3): Ecr08, 2003

Atypical hemoglobin H disease in a Thai patient resulting from a combination of alpha-thalassemia 1 and hemoglobin Constant Spring with hemoglobin J Bangkok heterozygosity. European Journal of Haematology 66(5): 312-316, 2001