130 related articles for article (PubMed ID: 29651217)
1. Coinheritance of Sicilian (δβ)
Eftekhari H; Pilehchian Langroudi M; Banihashemi A; Azizi M; Kamangar RY; Akhavan-Niaki H
Indian J Clin Biochem; 2018 Apr; 33(2):231-234. PubMed ID: 29651217
[TBL] [Abstract][Full Text] [Related]
2. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
Henderson SJ; Timbs AT; McCarthy J; Gallienne AE; Proven M; Rugless MJ; Lopez H; Eglinton J; Dziedzic D; Beardsall M; Khalil MS; Old JM
Hemoglobin; 2016; 40(2):75-84. PubMed ID: 26635043
[TBL] [Abstract][Full Text] [Related]
3. The phenomena of balanced effect between α-globin gene and of β-globin gene.
Zhong L; Gan X; Xu L; Liang C; Xie Y; Lin W; Chen P; Liu M
BMC Med Genet; 2018 Aug; 19(1):145. PubMed ID: 30119651
[TBL] [Abstract][Full Text] [Related]
4. Contrasting co-inheritance of alpha and beta mutations in delta beta thalassemia and hereditary persistence of fetal hemoglobin: a study from India.
Pandey H; Ranjan R; Singh K; Sharma A; Kishor K; Seth T; Saxena R
Hematology; 2018 Oct; 23(9):692-696. PubMed ID: 29621931
[TBL] [Abstract][Full Text] [Related]
5. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia.
Moassas F; Nweder MS; Murad H
BMC Pediatr; 2019 Feb; 19(1):61. PubMed ID: 30777047
[TBL] [Abstract][Full Text] [Related]
6. Molecular Study of Deletional and Nondeletional Mutations on the α-Globin Locus in the Azeri Population of Northwestern Iran.
Derakhshan SM; Khaniani MS; Afkhami F; PourFeizi AH
Hemoglobin; 2016 Sep; 40(5):319-322. PubMed ID: 27690152
[TBL] [Abstract][Full Text] [Related]
7. Compound heterozygosity for Hb Korle-Bu (beta(73); Asp-Asn) and Hb E (beta(26); Glu-Lys) with a 3.7-kb deletional alpha-thalassemia in Thai patients.
Changtrakun Y; Fucharoen S; Ayukarn K; Siriratmanawong N; Fucharoen G; Sanchaisuriya K
Ann Hematol; 2002 Jul; 81(7):389-93. PubMed ID: 12185510
[TBL] [Abstract][Full Text] [Related]
8. Coinheritance of hemoglobin D-Punjab and β
Panyasai S; Rahad S; Pornprasert S
Asian J Transfus Sci; 2017; 11(2):199-202. PubMed ID: 28970692
[TBL] [Abstract][Full Text] [Related]
9. Erythrocytosis in a child due to Hb Andrew-Minneapolis [β144(HC1)Lys→Asn (AAG>AAT or AAC)] associated with a Spanish (δβ)(0)-thalassemia.
Ropero P; González FA; Cela E; Beléndez C; Pérez B; Seri C; Fontanes E; Villegas A; Díaz-Mediavilla J
Hemoglobin; 2013; 37(1):48-55. PubMed ID: 23215953
[TBL] [Abstract][Full Text] [Related]
10. Dominantly Inherited beta-Thalassemia.
Efremov GD
Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
[TBL] [Abstract][Full Text] [Related]
11. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
Esteghamat F; Imanian H; Azarkeivan A; Pourfarzad F; Almadani N; Najmabadi H
Hemoglobin; 2007; 31(4):463-9. PubMed ID: 17994380
[TBL] [Abstract][Full Text] [Related]
12. Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs.
Fornari TA; Lanaro C; Albuquerque DM; Ferreira R; Costa FF
Exp Biol Med (Maywood); 2017 Feb; 242(3):267-274. PubMed ID: 27591578
[TBL] [Abstract][Full Text] [Related]
13. A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-Thalassemia.
Alauddin H; Kamarudin K; Loong TY; Azma RZ; Ithnin A; Jalil N; Razak NF; Koh-Xuan-Rong D; Ismail E; C-Khai L; Abdul Latiff Z; Alias H; Othman A
Hemoglobin; 2018 Jul; 42(4):247-251. PubMed ID: 30623696
[TBL] [Abstract][Full Text] [Related]
14. Identification of hemoglobin G-Philadelphia (alpha 68 Asn replaced by Lys) and hemoglobin Matsue-Oki (alpha 75 Asp replaced by Asn) in a black infant.
Yi-Tao Z; Headlee ME; Henson J; Lam H; Wilson JB; Huisman TH
Biochim Biophys Acta; 1982 Oct; 707(2):206-12. PubMed ID: 6814490
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. First Report of Association Between Rare α-Thalassemia Mutation (
Ghadami E; Tamaddoni A; Sedaghat S; Tabaripour R; Pourreza Baboli H; Akhavan-Niaki H
Indian J Clin Biochem; 2019 Jan; 34(1):115-117. PubMed ID: 30728682
[TBL] [Abstract][Full Text] [Related]
17. Molecular Characterization of β-Thalassemia Intermedia in Southeast Iran.
Miri-Moghaddam E; Bahrami S; Naderi M; Bazi A; Karimipoor M
Hemoglobin; 2016 Jun; 40(3):173-8. PubMed ID: 27117567
[TBL] [Abstract][Full Text] [Related]
18. Masking of a β-thalassemia determinant by a novel δ-globin gene defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301C>T] in Cis.
Colaco S; Trivedi A; Colah RB; Ghosh K; Nadkarni AH
Hemoglobin; 2014; 38(1):24-7. PubMed ID: 24200152
[TBL] [Abstract][Full Text] [Related]
19. Elevated Hb A₂ Levels in a Patient with a Compound Heterozygosity for the (β⁺) -31 (A > G) and (β⁰) Codon 17 (A > T) Mutations Together with a Single α-Globin Gene.
Panyasai S; Jaiping K; Pornprasert S
Hemoglobin; 2015; 39(4):292-5. PubMed ID: 26029792
[TBL] [Abstract][Full Text] [Related]
20. First Case of a Compound Heterozygosity for Two Nondeletional α-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze.
Zhou JY; Yan JM; Li J; Li DZ
Hemoglobin; 2016 Jun; 40(3):210-2. PubMed ID: 26956449
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
