These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
23. The alpha-globin gene adjacent to the gene for HbQ-alpha 74 Asp replaced by His is deleted, but not that adjacent to the gene for HbG-alpha 30 Glu replaced by Gln; three-fourths of the alpha-globin genes are deleted in HbQ-alpha-thalassemia. Lie-Injo LE; Dozy AM; Kan YW; Lopes M; Todd D Blood; 1979 Dec; 54(6):1407-16. PubMed ID: 508945 [TBL] [Abstract][Full Text] [Related]
25. 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]
26. Organization of alpha-globin genes in Hb Hasharon (alpha 47 asp replaced by his) carriers. Giglioni B; Comi P; Taramelli R; Ottolenghi S; Ciocca-Vasino MA; Anè C; Cappellini MD; Gianni AM Blood; 1980 Dec; 56(6):1145-9. PubMed ID: 6254584 [TBL] [Abstract][Full Text] [Related]
27. Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α(+)-thalassemia. Srivorakun H; Fucharoen G; Puangplruk R; Kheawon N; Fucharoen S Eur J Haematol; 2011 Jul; 87(1):68-72. PubMed ID: 21447006 [TBL] [Abstract][Full Text] [Related]
28. [Analysis of the non-deletion alpha-thalassemia mutations by PCR temperature gradient gel electrophoresis]. Zhao Y; Xu X; Yang Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):51-5. PubMed ID: 11172644 [TBL] [Abstract][Full Text] [Related]
29. Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy. Sanchaisuriya K; Chunpanich S; Fucharoen S; Fucharoen G; Sanchaisuriya P; Changtrakun Y Eur J Haematol; 2005 Mar; 74(3):221-7. PubMed ID: 15693792 [TBL] [Abstract][Full Text] [Related]
30. 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]
31. Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutation. Moumni I; Zorai A; Daoued BB; Mosbahi I; Omar S; Kaabachi N; Dellagi K; Abbes S Hemoglobin; 2007; 31(1):23-9. PubMed ID: 17365002 [TBL] [Abstract][Full Text] [Related]
32. Detection of beta-globin gene mutations by polymerase chain reaction. Lee HH; Chang JG; Lee LS; Lin ST; Ko TM; Choo KB Proc Natl Sci Counc Repub China B; 1991 Apr; 15(2):97-100. PubMed ID: 1682965 [TBL] [Abstract][Full Text] [Related]
33. A novel beta-delta globin gene fusion, anti-Lepore Hong Kong, leads to overexpression of delta globin chain and a mild thalassaemia intermedia phenotype when co-inherited with beta(0)-thalassaemia. So CC; Chan AY; Tsang ST; Lee AC; Au WY; Ma ES; Chan LC Br J Haematol; 2007 Jan; 136(1):158-62. PubMed ID: 17222202 [TBL] [Abstract][Full Text] [Related]
34. The alpha / beta and alpha 2 / alpha 1-globin mRNA ratios in different forms of alpha-thalassemia. Smetanina NS; Leonova JY; Levy N; Huisman TH Biochim Biophys Acta; 1996 Apr; 1315(3):188-92. PubMed ID: 8611658 [TBL] [Abstract][Full Text] [Related]
35. Identification of four novel delta-globin gene mutations in Greek Cypriots using polymerase chain reaction and automated fluorescence-based DNA sequence analysis. Trifillis P; Ioannou P; Schwartz E; Surrey S Blood; 1991 Dec; 78(12):3298-305. PubMed ID: 1742490 [TBL] [Abstract][Full Text] [Related]
37. Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine). Coleman MB; Lu ZH; Smith CM; Adams JG; Harrell A; Plonczynski M; Steinberg MH J Clin Invest; 1995 Feb; 95(2):503-9. PubMed ID: 7860732 [TBL] [Abstract][Full Text] [Related]
38. Analysis of the Hb M Milwaukee mutation at the DNA level. Horst J; Schäfer R; Kleihauer E; Kohne E Br J Haematol; 1983 Aug; 54(4):643-8. PubMed ID: 6307336 [TBL] [Abstract][Full Text] [Related]
39. A novel alpha-thalassemia nonsense mutation in codon 23 of the alpha2-globin gene (GAG-->TAG) in a Tunisian family. Siala H; Fattoum S; Messaoud T; Ouali F; Gerard N; Krishnamoorthy R Hemoglobin; 2004 Aug; 28(3):249-54. PubMed ID: 15481894 [TBL] [Abstract][Full Text] [Related]
40. Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia. Divoky V; Bissé E; Wilson JB; Gu LH; Wieland H; Heinrichs I; Prior JF; Huisman TH Biochim Biophys Acta; 1992 Dec; 1180(2):173-9. PubMed ID: 1463768 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]