289 related articles for article (PubMed ID: 32693657)
1. Mild Thalassemia Intermedia Due to Interaction of δβ-Thalassemia with Triplicated α-Globin Genes.
Payán-Pernía S; Bernal Noguera S; Rojas Rodríguez E; Serra Ferrer M; Remacha Sevilla ÁF
Hemoglobin; 2020 Jul; 44(4):294-296. PubMed ID: 32693657
[TBL] [Abstract][Full Text] [Related]
2. Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia.
Farashi S; Bayat N; Faramarzi Garous N; Ashki M; Montajabi Niat M; Vakili S; Imanian H; Zeinali S; Najmabadi H; Azarkeivan A
Hemoglobin; 2015; 39(3):201-6. PubMed ID: 26084319
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Double Heterozygosity for Hb Durham-N.C. (
Cannata M; Cassarà F; Vinciguerra M; Licari P; Passarello C; Leto F; Lo Pinto C; Pitrolo L; Ganci R; Maggio A; Giambona A
Hemoglobin; 2019 May; 43(3):210-213. PubMed ID: 31456457
[TBL] [Abstract][Full Text] [Related]
5.
Tamaddoni A; Khabaz Astaneh S; Tabaripour R; Akhavan-Niaki H
Hemoglobin; 2019 Jan; 43(1):12-17. PubMed ID: 30747024
[TBL] [Abstract][Full Text] [Related]
6. Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.
Prakobkaew N; Fucharoen S; Fuchareon G; Siriratmanawong N
Eur J Haematol; 2014 Jan; 92(1):73-9. PubMed ID: 24112054
[TBL] [Abstract][Full Text] [Related]
7. Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A
Satthakarn S; Panyasai S; Pornprasert S
Hemoglobin; 2020 Sep; 44(5):349-353. PubMed ID: 33023363
[TBL] [Abstract][Full Text] [Related]
8. Combination of Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G] and β
Li Y; Yan JM; Zhou JY; Lu YC; Li DZ
Hemoglobin; 2017 Jan; 41(1):47-49. PubMed ID: 28366026
[TBL] [Abstract][Full Text] [Related]
9. A Clinical Update of the Hb Siirt [β27(B9)Ala→Gly; HBB: c.83C>G] Hemoglobin Variant.
Cappabianca MP; Colosimo A; Sabatucci A; Dainese E; Di Biagio P; Piscitelli R; Sarra O; Zei D; Amato A
Hemoglobin; 2017 Jan; 41(1):53-55. PubMed ID: 28391745
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family.
Murad H; Moassas F
Hemoglobin; 2019 Jan; 43(1):66-68. PubMed ID: 30843739
[TBL] [Abstract][Full Text] [Related]
13. Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.
Azma RZ; Othman A; Azman N; Alauddin H; Ithnin A; Yusof N; Razak NF; Sardi NH; Hussin NH
Malays J Pathol; 2012 Jun; 34(1):57-62. PubMed ID: 22870600
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Hb A
Orts JA; Zúñiga Á; Bello Y; Fabregat AB; Vicente AI
Hemoglobin; 2016 Sep; 40(5):335-340. PubMed ID: 27535164
[TBL] [Abstract][Full Text] [Related]
16. A Novel Mutation of the α2-Globin Gene Causing α
Chen B; Lin L; Yi S; Chen Q; Wei H; Li G; Zheng C; He S; Qiu X
Hemoglobin; 2017 Jan; 41(1):56-58. PubMed ID: 28395547
[TBL] [Abstract][Full Text] [Related]
17. Genotype/Phenotype Correlation of β-Thalassemia in Syrian Patients: A Cross-Sectional Study.
Shoujaa A; Moasses F; Mukhalalaty Y; Murad H; Al-Quobaili F
Hemoglobin; 2020 Jan; 44(1):42-46. PubMed ID: 31903828
[TBL] [Abstract][Full Text] [Related]
18. Hb Westmead (
Jiang F; Ju AP; Li J; Chen GL; Zhou JY; Tang XW; Zuo LD; Li DZ
Hemoglobin; 2020 May; 44(3):153-155. PubMed ID: 32436451
[TBL] [Abstract][Full Text] [Related]
19. A Woman with Missing Hb A
Saller E; Knijnenburg J; Harteveld CL; Dutly F
Hemoglobin; 2020 May; 44(3):214-217. PubMed ID: 32605393
[TBL] [Abstract][Full Text] [Related]
20. Molecular Characterization and Hematological Aspects of Hb E-Myanmar [β26(B8)Glu→Lys and β65(E9)Lys→Asn,
Satthakarn S; Boonmee S; Panyasai S
Hemoglobin; 2020 Nov; 44(6):385-390. PubMed ID: 33222574
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]