330 related articles for article (PubMed ID: 29651865)
1. Compound Heterozygosity for Hb Alperton (HBB: c.407C>T) and IVS-I-5 (G>C) (HBB: c.92+5G>C) Mutations Presenting as a Moderate Anemia in an Indian Family.
Godbole KG; Ramachandran A; Karkamkar AS; Dalal AB
Hemoglobin; 2018 Mar; 42(2):141-142. PubMed ID: 29651865
[TBL] [Abstract][Full Text] [Related]
2. Hb Midnapore [β53(D4)Ala→Val; HBB: c.161C>T]: A Novel Hemoglobin Variant with a Structural Abnormality Associated with IVS-I-5 (G>C) (HBB: c.92+5G>C) Found in a Bengali Indian Family.
Panja A; Chowdhury P; Basu A
Hemoglobin; 2016 Sep; 40(5):300-303. PubMed ID: 27690257
[TBL] [Abstract][Full Text] [Related]
3. Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India.
Dehury S; Meher S; Patel S; Das K; Jana A; Bhattacharya S; Sahoo S; Sarkar B; Mohanty PK
Hemoglobin; 2019 Mar; 43(2):132-136. PubMed ID: 31190580
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. β-Thalassemia major resulting from compound heterozygosity for HBB: c.92+2T>C [formerly known as IVS-I-2 (T>C)] and a novel β(0)-thalassemia frameshift mutation: HBB: c.209delG; p.Gly70Valfs*20.
Kluge ML; Hoyer JD; Swanson KC; Oliveira JL
Hemoglobin; 2014; 38(4):292-4. PubMed ID: 24986053
[TBL] [Abstract][Full Text] [Related]
11. Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran.
Sajadpour Z; Amini-Farsani Z; Motovali-Bashi M; Yadollahi M; Khosravi-Farsani N
Hemoglobin; 2020 Jan; 44(1):27-30. PubMed ID: 31899996
[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. Description of a rare β-globin gene mutation, IVS-II-848 (C>A) (
Shoujaa A; Mukhalalaty Y; Murad H; Al-Quobaili F
Hemoglobin; 2019; 43(4-5):283-285. PubMed ID: 31718331
[TBL] [Abstract][Full Text] [Related]
14. β-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey.
Guzelgul F; Seydel GS; Aksoy K
Hemoglobin; 2020 Jul; 44(4):249-253. PubMed ID: 32664780
[TBL] [Abstract][Full Text] [Related]
15. The Spectrum of β-Thalassemia Mutations in a Population from the Brazilian Amazon.
Silva AN; Cardoso GL; Cunha DA; Diniz IG; Santos SE; Andrade GB; Trindade SM; Cardoso Mdo S; Francês LT; Guerreiro JF
Hemoglobin; 2016; 40(1):20-4. PubMed ID: 26372288
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent β-Thalassemia Mutations in the Tunisian Population.
Ben Charfeddine I; Ben Lazreg T; M'sakni A; Amara A; Mlika A; Chaïeb A; Hlel K; Zouari N; Zbidi F; Bouguila J; Soyah N; Ayedi A; Ben Hamouda H; Abroug S; Boughamoura L; Saad A; Gribaa M
Hemoglobin; 2015; 39(4):251-5. PubMed ID: 26016902
[TBL] [Abstract][Full Text] [Related]
20. IVS-II-16 (G>C) (
Uçucu S; Karabıyık T; Azik FM
Hemoglobin; 2021 Jul; 45(4):225-227. PubMed ID: 34396882
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
