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2. Hemoglobin E diseases: hematological, analytical, and biosynthetic studies in homozygotes and double heterozygotes for alpha-thalassemia. Wong SC; Ali MA Am J Hematol; 1982 Aug; 13(1):15-21. PubMed ID: 7137163 [TBL] [Abstract][Full Text] [Related]
3. Hb Westmead [alpha 122(H5)His----Gln], Hb E [beta 26(B8)Glu----Lys], and alpha-thalassemia-2 (3.7 Kb deletion) in a Laotian family. Gu YC; Gu LH; Wilson JB; Cepreganova B; Ramachandran M; Walker EL; Huisman TH; Potitong P Hemoglobin; 1991; 15(4):297-302. PubMed ID: 1787098 [No Abstract] [Full Text] [Related]
4. Globin synthesis in alpha- and beta-thalassemia. Ramot B; Ben-Bassat I; Mozel M; Shacked N Isr J Med Sci; 1973; 9(9):1469-74. PubMed ID: 4359643 [No Abstract] [Full Text] [Related]
5. Novel interactions of two α-Hb variants with SEA deletion α Srivorakun H; Singha K; Fucharoen G; Fucharoen S Hematology; 2018 Apr; 23(3):187-191. PubMed ID: 28945175 [TBL] [Abstract][Full Text] [Related]
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7. Hemoglobin Brest [beta 127 (H5)Gln----Lys] a new unstable human hemoglobin variant located at the alpha 1 beta 1 interface with specific electrophoretic behavior. Baudin-Chich V; Wajcman H; Gombaud-Saintonge G; Arous N; Riou J; Brière J; Galacteros F Hemoglobin; 1988; 12(2):179-88. PubMed ID: 3384710 [TBL] [Abstract][Full Text] [Related]
8. Hemoglobin Constant Spring, and unusual alpha-chain variant involved in the etiology of hemoglobin H disease. Clegg JB; Weatherall DJ Ann N Y Acad Sci; 1974; 232(0):168-78. PubMed ID: 4606609 [No Abstract] [Full Text] [Related]
9. Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G). Viprakasit V; Ekwattanakit S; Chalaow N; Riolueang S; Wijit S; Tanyut P; Chat-Uthai N; Tachavanich K Acta Haematol; 2014; 131(2):88-94. PubMed ID: 24081251 [TBL] [Abstract][Full Text] [Related]
10. Identification of Hb Lepore-Washington-Boston in association with Hb E [beta 26(B8)Glu----Lys] in a Thai female. Boontrakoonpoontawee P; Svasti J; Fucharoen S; Winichagoon P Hemoglobin; 1987; 11(4):309-16. PubMed ID: 3667318 [TBL] [Abstract][Full Text] [Related]
11. Hb H disease with various β hemoglobinopathies: molecular, hematological and diagnostic aspects. Fucharoen S; Fucharoen G Hemoglobin; 2012; 36(1):18-24. PubMed ID: 22145566 [TBL] [Abstract][Full Text] [Related]
12. 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. Dinçol G; Dinçol K; Erdem S; Pobedimskaya DD; Molchanova TP; Ye Z; Webber BB; Wilson JB; Huisman TH Hemoglobin; 1994 Jan; 18(1):57-60. PubMed ID: 8195009 [No Abstract] [Full Text] [Related]
13. Hemoglobin Riyadh--alpha2beta2 (120(GH3)Lys replaced by Asn). A new variant found in association with alpha-thalassemia and iron deficiency. El-Hazmi MA; Lehmann H Hemoglobin; 1976-1977; 1(1):59-74. PubMed ID: 1052171 [TBL] [Abstract][Full Text] [Related]
14. Molecular analysis of Hb Q-H disease and Hb Q-Hb E in a Singaporean family. Tan J; Tay JS; Wong YC; Kham SK; Bte Abd Aziz N; Teo SH; Wong HB Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():252-6. PubMed ID: 8629117 [TBL] [Abstract][Full Text] [Related]
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16. Hemoglobin H disease in two Iranian families. Rahbar S Clin Chim Acta; 1968; 20(3):381-5. PubMed ID: 5658939 [No Abstract] [Full Text] [Related]
17. A second family with Hb Minneapolis-Laos or alpha 2 beta (2)118(GH1)Phe----Tyr. Kleman K; Lubin B; Kutlar A; Wilson JB; Webber BB; Huisman TH Hemoglobin; 1987; 11(4):401-2. PubMed ID: 3667327 [No Abstract] [Full Text] [Related]
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