132 related articles for article (PubMed ID: 37815396)
1. Identification of two novel β-globin gene mutations HBB: exon3del, HBB: c.-81A>C.
Cao Y; Luo J
Hematology; 2023 Dec; 28(1):2265723. PubMed ID: 37815396
[TBL] [Abstract][Full Text] [Related]
2. The molecular characterization of Beta globin gene in thalassemia patients reveals rare and a novel mutations in Pakistani population.
Yasmeen H; Toma S; Killeen N; Hasnain S; Foroni L
Eur J Med Genet; 2016 Aug; 59(8):355-62. PubMed ID: 27263053
[TBL] [Abstract][Full Text] [Related]
3. [Molecular genetic characteristics of a family which coinheritance of rare-88 C>G (
Li W; Chen LT; Yu Y; Wang J; Li CY; Cai TE; Lu CJ; Li DX; Tian XJ
Zhonghua Yu Fang Yi Xue Za Zhi; 2023 Feb; 57(2):253-258. PubMed ID: 36797585
[TBL] [Abstract][Full Text] [Related]
4. Does size matter? Two new deletions in the HBB gene cause β
Ropero P; González Fernández FA; Nieto JM; Recasens V; Montañés Á; Murúzabal MJ; Sarasa M; Fernández C; Villegas A; Benavente CC
Ann Hematol; 2022 Jul; 101(7):1465-1471. PubMed ID: 35467101
[TBL] [Abstract][Full Text] [Related]
5. Co-heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia.
Vinciguerra M; Passarello C; Cassarà F; Leto F; Cannata M; Calvaruso G; Di Maggio R; Renda D; Maggio A; Giambona A
Int J Lab Hematol; 2016 Feb; 38(1):17-26. PubMed ID: 26418075
[TBL] [Abstract][Full Text] [Related]
6. Molecular and phenotype characterization of an elongated β-globin variant produced by HBB:C.313delA.
Lin W; Zhang Q; Shen Z; Qu X; Wang Q; Wei L; Qiu Y; Yang J; Xu X; Lao J
Int J Lab Hematol; 2021 Dec; 43(6):1620-1627. PubMed ID: 34271589
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Five novel globin gene mutations identified in five Chinese families by next-generation sequencing.
Zhang J; Xie M; Peng Z; Zhou X; Zhao T; Jin C; Yan Y; Zeng X; Li D; Zhang Y; Su J; Feng N; He J; Yao X; Lv T; Zhu B
Mol Genet Genomic Med; 2021 Dec; 9(12):e1835. PubMed ID: 34708592
[TBL] [Abstract][Full Text] [Related]
9. Case report: Identification of a novel triplication of alpha-globin gene by the third-generation sequencing: pedigree analysis and genetic diagnosis.
Chen Y; Xie T; Ma M; Yang J; Lv Y; Dong X
Hematology; 2023 Dec; 28(1):2277571. PubMed ID: 38059617
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A novel 15.8 kb deletion α-thalassemia confirmed by long-read single-molecule real-time sequencing: Hematological phenotypes and molecular characterization.
Zhong Z; Zhong G; Guan Z; Chen D; Wu Z; Yang K; Chen D; Liu Y; Xu R; Chen J
Clin Biochem; 2022 Oct; 108():46-49. PubMed ID: 35792184
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (
Hasan KN; Sufian A; Mazumder AK; Khaleque MA; Rahman M; Akhteruzzaman S
Hemoglobin; 2019 May; 43(3):162-165. PubMed ID: 31339392
[TBL] [Abstract][Full Text] [Related]
14. Characterization of a novel deletion causing beta-thalassemia major in an Afghan family.
Gallienne AE; Iberson NM; Dréau HM; Jackson H; Bignell PA; Old JM; Schuh A; Henderson SJ
Hemoglobin; 2010; 34(1):110-4. PubMed ID: 20113295
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of a rare β-thalassemia gene －90 (C>T) (HBB: c.-140 C>T) mutation associated with deletional Hb H disease (--
Qian H; Huang J; Xu J; Zhao W; Ye X; Liu W
Mol Genet Genomic Med; 2020 Nov; 8(11):e1472. PubMed ID: 32885601
[TBL] [Abstract][Full Text] [Related]
16. A novel 4.9 Kb deletion at beta-globin gene is identified by the third-generation sequencing: Case report from Baoan, China.
Chen X; Luo M; Pan L; Huang Y; Yan Z; Shen K; Mai G; Liang H; Li J; Chen Y; Xiong L
Clin Chim Acta; 2022 Apr; 529():10-16. PubMed ID: 35150653
[TBL] [Abstract][Full Text] [Related]
17. Combined Gap-Polymerase Chain Reaction and Targeted Next-Generation Sequencing Improve α- and β-Thalassemia Carrier Screening in Pregnant Women in Vietnam.
Lam TT; Nguyen DT; Le QT; Nguyen DA; Hoang DT; Nguyen HD; Nguyen CC; Doan KPT; Tran NT; Ha TMT; Trinh THN; Nguyen VT; Lam DT; Le MT; Nguyen XT; Ho TT; Tran TH; Ho VT; Bui TV; Nguyen VT; Hoang PB; Nguyen HT; Nguyen MH; Vo TB; Le DN; Truong TN; Dao HT; Vo PN; Nguyen TV; Tran NT; Tran QT; Van YT; Nguyen TT; Huynh BT; Nguyen TT; Tran KT; Nguyen CT; Doan PL; Nguyen TD; Do TT; Truong DK; Tang HS; Cao NT; Phan MD; Giang H; Nguyen HN
Hemoglobin; 2022 Jul; 46(4):233-239. PubMed ID: 35993587
[TBL] [Abstract][Full Text] [Related]
18. [Study of the types of mutations of Thalassemia in Shanghai area].
Gu Y; Wu B; Lu Y; Gu M; Lin J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Apr; 41(4):385-392. PubMed ID: 38565501
[TBL] [Abstract][Full Text] [Related]
19. Identification of Two Novel β-Thalassemia Mutations (HBB: c.335-346del and HBB: c.108 C > G) in Han Chinese.
Wang W; Wang Q; Tao T; Sun A; Ruan C; Chen S
Hemoglobin; 2015; 39(5):359-61. PubMed ID: 26096710
[TBL] [Abstract][Full Text] [Related]
20. First Report of a Novel Deletion Due to εγδβ-Thalassemia in a Chinese Family.
Hui ASY; Au PKC; Ting YH; Kan ASY; Cheng YKY; Leung AWK; Chan KYK; Li CK; Tang MHY; Leung TY
Hemoglobin; 2017 May; 41(3):175-179. PubMed ID: 28950778
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
