126 related articles for article (PubMed ID: 36898140)
1. Prevalence Rate of Thalassemia Carriers among Individuals with Microcytosis or Hypochromia in Portugal.
Santos D; Barreto M; Kislaya I; Mendonça J; P Machado M; Lopes P; Matias Dias C; Faustino P
Acta Med Port; 2023 Jul; 36(7-8):467-474. PubMed ID: 36898140
[TBL] [Abstract][Full Text] [Related]
2. Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH.
Blattner A; Brunner-Agten S; Ludin K; Hergersberg M; Herklotz R; Huber AR; Röthlisberger B
Blood Cells Mol Dis; 2013 Jun; 51(1):39-47. PubMed ID: 23491071
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. High prevalence of alpha-thalassemia among individuals with microcytosis and hypochromia without anemia.
Borges E; Wenning MR; Kimura EM; Gervásio SA; Costa FF; Sonati MF
Braz J Med Biol Res; 2001 Jun; 34(6):759-62. PubMed ID: 11378664
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Molecular epidemiological analysis of α- and β-thalassemia in Fujian province].
Xu LP; Huang HL; Wang Y; Zheng L; Wang LS; Xu JB; Huang XX; Lin Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):403-6. PubMed ID: 23926004
[TBL] [Abstract][Full Text] [Related]
8. Prevalence of 3.7 and 4.2 deletions in Sudanese patients with red cells hypochromia and microcytosis.
Osman HA; Hamid MMA; Ahmad RB; Saleem M; Abdallah SA
BMC Res Notes; 2020 Feb; 13(1):65. PubMed ID: 32041645
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Screening for common β-globin gene cluster deletions in Chinese individuals with increased hemoglobin F.
Cai WJ; Li J; Xie XM; Li DZ
Int J Lab Hematol; 2015 Dec; 37(6):752-7. PubMed ID: 26179971
[TBL] [Abstract][Full Text] [Related]
12. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
Zhu BS; He J; Zhang J; Zeng XH; Su J; Xu XH; Li SY; Chen H; Zhang YH
Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
[TBL] [Abstract][Full Text] [Related]
13. Molecular analysis of complex cases of alpha- and beta-thalassemia in Mexican mestizo patients with microcytosis and hypochromia reveals two novel alpha(0) -thalassemia deletions - -(Mex1) and - -(Mex2).
de-la-Cruz-Salcedo EI; Ibarra B; Rizo-de-la-Torre LC; Sánchez-López JY; González-Mercado A; Harteveld CL; Perea-Díaz FJ
Int J Lab Hematol; 2016 Oct; 38(5):535-42. PubMed ID: 27339814
[TBL] [Abstract][Full Text] [Related]
14. A novel (A)γδβ(0)-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization.
Singha K; Fucharoen G; Hama A; Fucharoen S
Clin Biochem; 2015 Jul; 48(10-11):703-8. PubMed ID: 25866400
[TBL] [Abstract][Full Text] [Related]
15. Effect of deletions in the α-globin gene on the phenotype severity of β-thalassemia.
Saha D; Chowdhury PK; Panja A; Pal D; Nayek K; Chakraborty G; Sharma P; Das R; Basu S; Chatterjee R; Basu A
Hemoglobin; 2022 Mar; 46(2):118-123. PubMed ID: 36000542
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A novel 223 kb deletion in the beta-globin gene cluster was identified in a Chinese thalassemia major patient.
Zhu F; Wei X; Cai D; Pang D; Zhong J; Liang M; Zuo Y; Xu X; Shang X
Int J Lab Hematol; 2019 Aug; 41(4):456-460. PubMed ID: 30945812
[TBL] [Abstract][Full Text] [Related]
18. Heterozygous beta-thalassemia: not infrequent in Mexico.
Ruiz-Argüelles GJ; López-Martínez B; Ruiz-Reyes G
Arch Med Res; 2001; 32(4):293-5. PubMed ID: 11440786
[TBL] [Abstract][Full Text] [Related]
19. Prevalence and Genetic Analysis of
Nezhad FH; Nezhad KH; Choghakabodi PM; Keikhaei B
J Epidemiol Glob Health; 2018 Dec; 8(3-4):189-195. PubMed ID: 30864762
[TBL] [Abstract][Full Text] [Related]
20. Next-generation sequencing improves thalassemia carrier screening among premarital adults in a high prevalence population: the Dai nationality, China.
He J; Song W; Yang J; Lu S; Yuan Y; Guo J; Zhang J; Ye K; Yang F; Long F; Peng Z; Yu H; Cheng L; Zhu B
Genet Med; 2017 Sep; 19(9):1022-1031. PubMed ID: 28125089
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
