+ 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 the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and beta-thalassemia or Hb Sabine confirms the functional role of the Agamma -158 C>T mutation in gamma-globin gene transcription



Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and beta-thalassemia or Hb Sabine confirms the functional role of the Agamma -158 C>T mutation in gamma-globin gene transcription



Blood Cells, Molecules and Diseases 41(3): 263-264




Please choose payment method:






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

Accession: 052269088

Download citation: RISBibTeXText

PMID: 18718799

DOI: 10.1016/j.bcmd.2008.05.009


Related references

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

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

The Cretan type of non-deletional hereditary persistence of fetal hemoglobin [A gamma-158C-->T] results from two independent gene conversion events. Human Genetics 102(6): 629-634, 1998

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

A non-deletional form of hereditary persistence of fetal hemoglobin due to a novel C fwdarw T mutation at nucleotide-158, 5 to the cap site of the A-gamma human globin gene. Blood 86(10 SUPPL 1): 486A, 1995

Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant. Blood 77(4): 861-867, 1991

G gamma A gamma (beta+) hereditary persistence of fetal hemoglobin: the G gamma -158 C-->T mutation in cis to the -175 T-->C mutation of the A gamma-globin gene results in increased G gamma-globin synthesis. American Journal of Hematology 42(2): 186-190, 1993

Analysis of deletional hereditary persistence of fetal hemoglobin/δβ-thalassemia and δ-globin gene mutations in Southerwestern China. Molecular Genetics and Genomic Medicine 2019: E706, 2019

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

Non-deletional hereditary persistence of fetal hemoglobin -158 CfwdarwT promoter mutation in homozygous beta thalassemia. Blood 98(11 Part 2): 21b, November 16, 2001

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

Expression of human globin genes in transgenic mice carrying the beta-globin gene cluster with a mutation causing G gamma beta + hereditary persistence of fetal hemoglobin. Annals of the New York Academy of Sciences 612: 167-178, 1990

Expression of human globin genes in transgenic mice carrying the beta globin gene cluster with a mutation causing g gamma beta positive hereditary persistence of fetal hemoglobin. Bank, A (Ed ) Annals Of The New York Academy Of Sciences, Vol 612 Sixth Cooley's Anemia Symposium; New York, New York, Usa, March 13-15, Xiii+590p New York Academy Of Sciences: New York, New York, Usa Illus Maps 167-178, 1990

Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks. Blood 67(2): 551-554, 1986

Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black population. Blood 64(6): 1292-1296, 1984