594 related articles for article (PubMed ID: 24471655)
1. A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A].
Moumni I; Zorai A; Mahjoub S; Mosbahi I; Chaouechi D; Benromdhane N; Abbes S
Hemoglobin; 2014; 38(2):88-90. PubMed ID: 24471655
[TBL] [Abstract][Full Text] [Related]
2. Mutational spectrum of delta-globin gene in the Portuguese population.
Morgado A; Picanço I; Gomes S; Miranda A; Coucelo M; Seuanes F; Seixas MT; Romão L; Faustino P
Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
[TBL] [Abstract][Full Text] [Related]
3. Normal Hb A2 β-thalassemia trait: frameshift mutation (HBB: c.187_251dup) in cis with the Hb A2' δ-globin gene missense mutation (HBD: c.49G>C).
Waye JS; Eng B; Hellens L; Hohenadel BA; Nakamura LM; Walker L
Hemoglobin; 2013; 37(2):201-4. PubMed ID: 23398055
[TBL] [Abstract][Full Text] [Related]
4. 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]
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. Hb A2 Hong Kong - A novel δ-globin variant in a Chinese family masks the diagnosis of β-thalassemia trait.
So CC; Chan AY; Luo HY; Verhovsek M; Chui DH; Ling SC; Chan LC
Hemoglobin; 2011; 35(2):162-5. PubMed ID: 21417575
[TBL] [Abstract][Full Text] [Related]
7. New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG].
Phylipsen M; Harteveld CL; de Metz M; Gallivan MV; Arkesteijn SG; Luo HY; Chui DH; Giordano PC
Hemoglobin; 2010; 34(5):445-50. PubMed ID: 20854118
[TBL] [Abstract][Full Text] [Related]
8. A New δ-Globin Gene Variant: Hb A2-Fengshun [δ121(GH4)Glu→Lys (HBD: c.364G > A)].
Yan JM; Zhou JY; Xie XM; Li J; Li DZ
Hemoglobin; 2016 Jun; 40(3):213-4. PubMed ID: 27117573
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Coinheritance of a Rare Nucleotide Substitution on the β-Globin Gene and Other Known Mutations in the Globin Clusters: Management in Genetic Counseling.
Vinciguerra M; Passarello C; Leto F; Crivello A; Fustaneo M; Cassarà F; Cannata M; Maggio A; Giambona A
Hemoglobin; 2016 Aug; 40(4):231-5. PubMed ID: 27258795
[TBL] [Abstract][Full Text] [Related]
11. A New δ-Globin Gene Variant: Hb A2-Yulin [δ46(CD5)Gly→Arg,
Lin HM; Liang L; Cai YJ; Zheng LH; Qin QP; Li YQ
Hemoglobin; 2024 Mar; 48(2):121-124. PubMed ID: 38450437
[TBL] [Abstract][Full Text] [Related]
12. Association of Hb A
Panyasai S; Pornprasert S
Hemoglobin; 2020 May; 44(3):179-183. PubMed ID: 32482156
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in Iran.
Amirian A; Karimipoor M; Jafarinejad M; Taghavi M; Kordafshari A; Fathi Azar S; Mohammadi MS; Zeinali S
Arch Iran Med; 2011 Jan; 14(1):8-11. PubMed ID: 21194254
[TBL] [Abstract][Full Text] [Related]
15. Molecular Characterization of δ-Thalassemia in Iran.
Kordafshari A; Amirian A; Zeinali S; Valaei A; Maryami F; Karimipoor M
Hemoglobin; 2016; 40(1):44-7. PubMed ID: 26754299
[TBL] [Abstract][Full Text] [Related]
16. A Case Report of Compound Heterozygosity for β
Intasai N; Phasit A; Panyasai S; Pornprasert S
Hemoglobin; 2019 Jan; 43(1):63-65. PubMed ID: 31037981
[TBL] [Abstract][Full Text] [Related]
17. Comprehensive spectrum of the β-Thalassemia mutations in Khuzestan, southwest Iran.
Galehdari H; Salehi B; Azmoun S; Keikhaei B; Zandian KM; Pedram M
Hemoglobin; 2010; 34(5):461-8. PubMed ID: 20854120
[TBL] [Abstract][Full Text] [Related]
18. Hb A2-Konz [δ50(D1)Ser → Thr; HBD: c.151T > A]: a new δ chain hemoglobin variant characterized by mass spectrometry and high performance liquid chromatography.
Alayi TD; Van Dorsselaer A; Epting T; Bissé E; Schaeffer-Reiss C
Hemoglobin; 2014; 38(2):133-6. PubMed ID: 24471805
[TBL] [Abstract][Full Text] [Related]
19. First description of a Hb A2 variant in Thailand. Identification of Hb A2-Melbourne [δ43(CD2)Glu→Lys] in Thai individuals.
Chaibunruang A; Fucharoen G; Fucharoen S
Hemoglobin; 2012; 36(1):80-4. PubMed ID: 21967556
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
