β-thalassemia in Turkey: A review of the clinical, epidemiological, molecular, and evolutionary aspects

Hemoglobin

Volumn 25, Issue 2, 2001, Pages 227-239

  Tadmouri, G O ^a   Basak A N ^a  

^a BOGAZICI UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

BETA THALASSEMIA; CONFERENCE PAPER; EVOLUTION; GEOGRAPHIC DISTRIBUTION; HUMAN; MARRIAGE; TURKEY (REPUBLIC);

BETA-THALASSEMIA; EVOLUTION; FEMALE; HISTORY, 20TH CENTURY; HISTORY, ANCIENT; HISTORY, MEDIEVAL; HISTORY, MODERN 1601-; HUMANS; MALE; PREGNANCY; PRENATAL DIAGNOSIS; PREVALENCE; TOPOGRAPHY, MEDICAL; TURKEY;

EID: 0034946844     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.1081/HEM-100104031     Document Type: Conference Paper

References (92)

1. Community control of hereditary anemias: Memorandum from a WHO meeting
2. The history of β-thalassemia in Turkey
3. Thalassaemia minor with large amount of fetal haemoglobin: Report of four cases
4. The thalassaemia syndromes: V. Cooley's anaemia with low level of fetal hemoglobin: A genetic study in four families
5. Growth and sexual maturation in children with thalassemia major
6. Thalassaemia intermedia: A genetic study in 11 patients
7. Molecular heterogeneity of β-thalassemia intermedia in Turkey
8. The incidence of β-thalassaemia and abnormal hemoglobin in Turkey
9. 2 in Turkey: Study in Heterozygotes
10. 2 β-thalassemia in the province of Denizli
11. +-thalassemia, glucose-6-phosphate dehydrogenase deficiency and haptoglobin types in Turks from Western Thrace
12. 2 β-thalassemia in the province of Mustafakemalpaşa/Bursa, Turkey
13. Prevalence of beta-thalassaemia trait in 1124 students from aegean region of Turkey
14. Frequencies of some blood disorders in Nazilli
15. Distribution of hemoglobinopathies in Turkey: Based on studies conducted at Hacettepe Children's Hospital and reviews of other studies
16. Hemoglobinopathies in the district of Antalya, Turkey
17. Review of a 4.5 years research at the Thalassemia Center of Antalya
18. Survey on haemoglobin variants, β-thalassaemia, glucose-6-phosphate dehydrogenase deficiency and haptoglobint types in Turkish people living in Manavgat, Serik and Boztepe (Antalya)
19. The frequency of anaemia, iron deficiency, hemoglobin S and β-thalassemia in the South of Turkey
20. Abnormal hemoglobins and thalassemias in the region of Çukurova
21. Premarital screening for hemoglobinopathies in Hatay
22. Screening of abnormal hemoglobins in the City of Kahramanmaraş
23. Hemoglobin S and some other hemoglobinopathies in Eti-Turks
24. Van golu cevresinde beta talasemi tasiyiciligi sikligi
25. Hereditary persistence of fetal hemoglobin and β-thalassemia in a Turkish Child
26. Gamma-chain heterogeneity of fetal hemoglobin in non-black β- and δβ-thalassemia and HPFH heterozygotes and homozygotes
27. α-thalassemia and β-thalassemia in a Turkish family
28. 0-Thalassemia Traits
29. Immerslund grasbeck syndrome coexisting with β-thalassemia trait
30. Fanconi aplastic anemia associated with β-thalassemia trait
31. Homozygous β-thalassemia associated with familial mediterranean fever in a Turkish patient
32. Hemoglobin H-β-thalassemia
33. Haemoglobin O Arab (β121 Glu → Lys) in Turkish Cypriot Population
34. 0-Thalassemia
35. Molecular basis and prenatal diagnosis of hemoglobinopathies in Turkey
36. Compound heterozygosity for hemoglobin Knossos β27(B9)Ala → -Ser and IVS-I-1 Mutation
37. A further note on the combination of an α chain variant with β-thalassemia
38. The thalassaemia syndromes. VI. Two subtypes of sickle cell-beta thalassaemia disease: (a) Normocytic type of sickle cell-beta thalassaemia disease; (b) microcytic type of sickle cell-beta thalassaemia disease
39. Genotype-phenotype analysis in HbS-β-thalassemia
40. β-thalassaemia mutations in the turkish population
41. Mild and severe β-thalassemia among homozygotes from Turkey: Identification of the types by hybridization of amplified DNA with synthetic probes
42. Molecular Basis of β-thalassemia in Turkey: Detection of rare mutations by direct sequencing
43. β-thalassemia in Turkey
44. The molecular basis of β-thalassemia in Turkey
45. Regional distributions of β-thalassemia mutations in Turkey
46. β-thalassemia alleles in aegean region of Turkey: Effect on clinical severity of disease
47. Molecular and population genetic analyses of β-thalassemia in Turkey
48. 230(B12)Arg → Thr, a variant associated with β-thalassemia due to a G → C substitution adjacent to the donor splice site of the first intron
49. β-thalassemia due to a T → A mutation within the ATA box
50. The G → A mutation at position + 22 3′ to the cap site of the β-globin gene as a possible cause for a β-thalassemia
51. Nonsense and frameshift mutations in β-thalassemia detected in cloned β-globin genes
52. A novel deletion in a Turkish β-thalassemia patient detected by DGGE and direct sequencing: FSC 22-24 (- 7bp)
53. Two rare mutations [Cd 30 (G → C) and CDs 36/37 (-T)] in a Turkish thalassemia major patient from Bulgaria
54. Evolution of a geneticd disease in an ethnic isolate: β-thalassemia in the Jews of Kurdistan
55. A rare mutation [IVS-I-130 (G → A)] in a Turkish β-thalassemia major patient
56. β-thalassemia gene analysis in a Turkish family reveals a 7 bp deletion in the coding region
57. 0-thalassemia in a Turkish patient
58. β-thalassaemia in the immigrant and non-immigrant German populations
59. A novel 13 bp deletion in the 3′UTR of the β-globin gene causes β-thalassemia in a Turkish patient
60. A mild thalassemia major resulting from a compound heterozygosity for the IVS-11-1 (G → A) mutation and the rare T → C mutation at the polyadenylation site
61. An ∼300 bp deletion involving part of the 5′ β-globin gene region is observed in members of a Turkish family with β-thalassemia
62. A New Turkish type of β-thalassaemia major with homozygosity for two non-consecutive 7.6 kb deletion of the ψβand β genes and an intact δ gene
63. A novel (δβ)(0)-thalassemia due to a approximately 30-kb deletion observed in a Turkish family
64. The thalassemia repository
65. The β- and δ-thalassemia repository
66. The β- and δ-thalassemia repository (seventh edition)
67. The β- and δ-thalassemia repository (eighth edition)
68. A C → T Substitution at nt - 101 in a conserved DNA sequence of the promoter region of the β-globin gene is associated with "silent$ β-thalassemia
69. A rare β-thalassemia mutation in a Turkish patient: FSC 36/37 (-T)
70. Rare β-thalassemia mutation IVS-II-848 (C → A) first reported in a Turkish Cypriot family
71. 2 and F in a Turkish family
72. Identification of the "Chinese" IVS-II-654 (C → T) β-thalassemia mutation in an immigrant Turkish family: Recurrence or migration?
73. 0-thalassemia intermedia
74. 0 thalassaemia
75. Prenatal diagnosis of hemoglobinapathies in Turkey: Hacettepe experience
76. Prenatal diagnosis of β-thalassaemia and sickle cell anaemia in Turkey
77. Consanguineous marriages in the Turkish population
78. Premarital screening of hemoglobinopathies: A pilot study in Turkey
79. β-thalassemia problems in the Turkish population in the F.R.G
80. The rate of mutations of human genes
81. Malaria and ecosystems: From prehistory to posteradication
82. Porotic hyperostosis, anemias malarias, and marshes in the prehistoric eastern mediterranean
83. Malaria in the eastern mediterranean in prehistory and antiquity
84. Recognition of sickle cell anemia in skeletal remains of children
85. Sequence analysis reveals a β-thalassaemia mutation in the DNA of skeletal remains from the archaeological site of Akhziv, Israel