×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
GeneticVariation
CLINVAR
Variable phenotypes of sickle cell disease in India with the Arab-Indian haplotype.
25135424
2015
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
First Detection of a Splice Site β-Thalassemia Mutation, IVS-I-6 (T > C) (HBB: c.92 + 6T > C) in a Chinese Family.
25856402
2015
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Molecular Scanning of β-Thalassemia in the Southern Region of Central Java, Indonesia; a Step Towards a Local Prevention Program.
26291967
2015
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Genotype-phenotype correlation and report of novel mutations in β-globin gene in thalassemia patients.
25976460
2015
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
GeneticVariation
CLINVAR
Genotype-phenotype correlation and report of novel mutations in β-globin gene in thalassemia patients.
25976460
2015
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
β-Globin Mutations in Egyptian Patients With β-Thalassemia.
25617386
2015
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Novel Βeta (β)-Thalassemia Mutation in Turkish Children.
25825561
2015
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Broader spectrum of β-thalassemia mutations in Oman: regional distribution and comparison with neighboring countries.
25677748
2015
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Tetra-Primer ARMS PCR Optimization for Detection of IVS-II-I (G-A) and FSC 8/9 InsG Mutations in β-Thalassemia Major Patients in Isfahan Population.
25905082
2015
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Spectrum of Beta Globin Gene Mutations in Egyptian Children with β-Thalassemia.
25408857
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Frequency of beta-thalassemia or beta-hemoglobinopathy carriers simultaneously affected with alpha-thalassemia in Iran.
25016698
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
GeneticVariation
CLINVAR
Molecular epidemiological characterization and health burden of thalassemia in Jiangxi Province, P. R. China.
25000193
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Hb Knossos: HBB:c.82G>T Associated with HBB:c.315+1G>A Beta Zero Mutation Causes Thalassemia Intermedia.
25332589
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
GeneticVariation
CLINVAR
Coexistence of two β-globin gene deletions in a Chinese girl with β-thalassemia minor.
24200214
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
GeneticVariation
CLINVAR
The spectrum of β-thalassemia mutations in Hatay, Turkey: reporting three new mutations.
25155404
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Molecular basis of transfusion dependent beta-thalassemia major patients in Sabah.
24369358
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results.
25087612
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
The spectrum of β-thalassemia mutations in Hatay, Turkey: reporting three new mutations.
25155404
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Molecular characterization of α- and β-thalassaemia among Malay patients.
24857915
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Hemoglobin Constant Spring is markedly high in women of an ethnic minority group in Vietnam: a community-based survey and hematologic features.
24368026
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
GeneticVariation
CLINVAR
β -thalassemia intermedia in Northern Iraq: a single center experience.
24719849
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Coexistence of two β-globin gene deletions in a Chinese girl with β-thalassemia minor.
24200214
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
High resolution melting analysis: a rapid screening and typing tool for common β-thalassemia mutation in Chinese population.
25089872
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Molecular update of β-thalassemia mutations in the Syrian population: identification of rare β-thalassemia mutations.
24828949
2014
×
Entrez Id:
3043
Gene Symbol:
HBB
HBB
beta Thalassemia
0.800
CausalMutation
CLINVAR
Molecular diagnostics of the HBB gene in an Omani cohort using bench-top DNA Ion Torrent PGM technology.
24880717
2014