Abnormal hemoglobins in Turkey

Turkish Journal of Haematology

Volumn 19, Issue 1, 2002, Pages 63-74

  Altay, Çiǧdem ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

Author keywords

Abnormal hemoglobin; Turkey

Indexed keywords

HEMOGLOBIN ALPHA CHAIN; HEMOGLOBIN BETA CHAIN; HEMOGLOBIN C; HEMOGLOBIN DERIVATIVE; HEMOGLOBIN E; HEMOGLOBIN VARIANT;

ALPHA CHAIN; BETA CHAIN; BETA THALASSEMIA; CLINICAL RESEARCH; DISEASE CARRIER; DISEASE CLASSIFICATION; DISEASE SEVERITY; HEMOGLOBIN ANALYSIS; HEMOGLOBIN DETERMINATION; HEMOGLOBINOPATHY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HOMOZYGOSITY; HUMAN; IMMIGRANT; MASS SCREENING; POPULATION RESEARCH; REVIEW; TURKEY (REPUBLIC);

EID: 0036212984     PISSN: 13007777     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (87)

1. Abnormal hemoglobins and thalassemia in Turkey
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3. HbE syndromes. 1. HbE in Eti Turks
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5. The first observation of HbS and E disease
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10. Survey on haemoglobin variants, beta-thalassemia, glucose-6-phosphate dehydrogenase deficiency and haptoglobin types in Turkish people living in Manavgat, Serik and Boztepe (Antalya)
11. Hemoglobinopathies in Turkey
12. Hemoglobin hamadan or alpha 2 beta 256 (D7) Gly---Arg in a Turkish family
13. Hb Beograd-beta zero thalassemia in a Turkish family from Yugoslavia
14. Compound heterozygosity for HbE Saskatoon or alpha 2 beta 22 (B4) Glu-Lys and beta-thalassemia type IVSI-6 (T-C)
15. Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27 (B9) Ala-Ser] and of Hb City of Hope [beta 69 (E13) Gly-Ser] with beta (0)-thalassemia
16. Some notes about HbQ India and HbQ İran
17. Antakya'nin iki Eti Türkü köyünde anormal hemoglobinler ve A2' si yüksek beta talasemi
18. Sickle cell anaemia among Eti-Turks: Haematological, clinical and genetic observations
19. Homozygous hemoglobin D Punjab
20. HbD punjab-alpha thalassaemia combination in a Turkish family
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23. Hemoglobin S and some other hemoglobinopathies in Eti-Turks
24. Adana bölgesinde bebeklerde kordon kani çalişmasi ile alfa talasemi G6PD enzim eksikliǧi ve HbS sikliǧinin araştirilmasi
25. Population studies of HbS and other variants in Çukurova. The southern part of Turkey
26. Abnormal hemoglobins in Turkish Cypriots
27. Prevalence of thalassemia and G6PD deficiency in North Cyprus
28. Mustafa Kemal Paşa ve köylerinde anormal Hb ve HbA2 yüksekliǧi ile karakterize beta-thalassemia taşiyiciliǧi araştirmasi
29. Screening of abnormal hemoglobins and high HbA2 beta-thalassemia in Elbistan area
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31. Hemoglobinopathies in the district of Antalya, Turkey
32. Muǧla ili ve çevresinde talasemia ve anormal hemoglobin Taramasi
33. Analysis of thalassemia syndromes and abnormal hemoglobins in patients from the aegean region of Turkey
34. Hemoglobin İstanbul: Substitution of glutamine for histidine in a proximalhistidine (F8(92))
35. Hb Summerhill or alpha 2 B2 52 (D3) Asp-His in a Turkish family from Cyprus
36. Hemoglobin O-Padova or alpha (2) 30 (B11) Glu-Lys beta 2 observed in members of a Turkish family
37. HbJ Antakya or alpha 2 beta (2) 65 (E9) Lys-Met in a Turkish family and Hb complutense or alpha 2 beta (2) 127 (H5) Gln-Glu in a Spanish family; Correction of a previously published identification
38. HbP Nilotic or alpha 2 (beta delta) 2 in a Turkish family
39. HbN Baltimore [alpha 2 beta 2 (95) (FG2) Lys-Glu] and HbJ İran [alpha 2 beta 2 (77) (Ef1) His-Asp] observed in a Turkish family from Antalya
40. Hb Adana or alpha 2 (59) (E8) Gly→Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the-(alpha) 20.5 Kb alpha-thal-1 deletion in two Turkish patients
41. Hb Hakkari or alpha 2 beta 2 31 (B13) Leu→Arg, a severely unstable hemoglobin variant associated with numerous intra-erythroblastic inclusions and erythroid hyperplasia of the bone marrow
42. Hemoglobin Köln β98 (FG5) Val→Met. In a Turkish child
43. Hb Antalya [codons 3-5 (Leu-Thr-Pro→Ser-Asp-Ser)]: A new unstable variant leading to chronic microcytic anemia and high HbA2
44. Hb Moabit, α86 (D7) Leu-Arg. A new unstable abnormal Hb
45. A syllabus of human hemoglobin variants
46. HbJ Anatolia [alpha 61 (E10) Lys-Thr]: Structural characterization and gene localization of a new alpha chain variant
47. Hemoglobin Ube-2 (alpha 68 Asn-Asp) observed in a Turkish family
48. Congenital methemeoglobinemia due to hemoglobin M
49. Hb Capa or alpha (2) 94 (G1) Asp→Gly beta 2, a mildly unstable variant with an A→G (GAC→GGC) mutation in codon 94 of the alpha 1-globin gene
50. Hemoglobin G Georgia in a Turkish family in the Netherlands
51. Hb Strumica. α112 (G19) His→Arg (CAC→CGC) in a Turkish family
52. A case of HB J-Meerut (or HbJ Birmingham) [alpha 120 (H3) Ala→Glu]
53. Hemoglobin C-beta (0) thalassemia
54. A new HbJ from Turkey. Hb Ankara (B10A-7Ala-Asp)
55. Homozygosity for HbE Saskatoon [beta22 (B4) Glu→Lys] in a Turkish patient
56. HbG Coushatta or β22 (B4) Glu→Ala in a Turkish male
57. HbG Coushatta β22 (B4) Glu→Ala in a Turkish family
58. 227 (B9) Ala-Ser] and IVSI-1 mutation
59. First observation of HbJ İran B77 (EF1) His-Asp in Turkey
60. Haemoglobin G-Szuhu, beta80 Asn-Lys, in the homozygous state in a patient with abetalipoproteinaemia
61. A survey for hemoglobin variants and high HbA2 beta-thalassemia in 1000 Turks
62. Homozygous HbD Punjab disease
63. HbD Los Angeles/B IVSI-110 (G-A) combination in a Turkish woman
64. Homozygosity for hemoglobin O Arab
65. Haemoglobin O Arab (B121 Glu-Lys) in Turkish Cypriot population
66. Hb Brockton [alpha 2 beta 2138 (H16) Ala----Pro] observed in a Turkish girl
67. HbF Baskent or alpha 2A gamma 128 (H6) Ala----Thr
68. Hemoglobin Lepore Boston in a Turkish family
69. Beta-talasemi ve Hb Lepore Boston 'un birlikte bulunduǧu bir vaka
70. Konya ve Denizli yöresinde beta-talasemi sikliǧi
71. Alpha-thalassemia and beta-thalassemia in a Turkish family
72. A novel delta 0 mutation in cis with Hb Knossos: A study of different genetic interactions in three Egyptian families
73. Molecular analysis of turkish beta-thalassemia heterozygotes with normal HbA2 levels
74. Further example of hemoglobin D in Turkish family
75. Sequence variations in the 5′ hypersensitive site-2 of the locus control region of beta S chromosomes are associated with different levels of fetal globin in hemoglobin S homozygotes
76. Genotype-phenotype analysis in HbS-beta-thalassemia
77. Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Turkey
78. Identification of HbD Punjab gene: Application of DNA amplification in the study of abnormal hemoglobins
79. A new hemoglobin variant resembling hemoglobin E. Hemoglobin E Saskatoon: Beta-22 Glu replaced by Lys
80. Molecular characterization of HbS(C) beta-thalassemia in American blacks
81. Combinations of beta chain abnormal hemoglobins with each other or with beta-thalassemia determinants with known mutations: Influence on phenotype