155 related articles for article (PubMed ID: 32190157)
1. Identification of seven novel variants in the β-globin gene in transfusion-dependent and normal patients.
Aldakeel SA; Ghanem NZ; Al-Amodi AM; Osman AK; Al Asoom LI; Ahmed NR; Almandil NB; Akhtar MS; Azeez SA; Borgio JF
Arch Med Sci; 2020; 16(2):453-459. PubMed ID: 32190157
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. [Rare thalassemia caused by novel nucleotide variants in the globin gene: four case reports and literature review].
Da ZZ; Chen LH; Jiang HM; Wang GP
Zhonghua Xue Ye Xue Za Zhi; 2021 Apr; 42(4):313-317. PubMed ID: 33979976
[No Abstract] [Full Text] [Related]
5.
Borgio JF; AbdulAzeez S; Al-Muslami AM; Naserullah ZA; Al-Jarrash S; Al-Suliman AM; Al-Madan MS; Al-Ali AK
Arch Med Sci; 2018 Jan; 14(1):230-236. PubMed ID: 29379553
[TBL] [Abstract][Full Text] [Related]
6. A comprehensive review of the prevalence of beta globin gene variations and the co-inheritance of related gene variants in Saudi Arabians with beta-thalassemia.
Alaithan MA; AbdulAzeez S; Borgio JF
Saudi Med J; 2018 Apr; 39(4):329-335. PubMed ID: 29619482
[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. Co-inheritance of alpha globin gene deletion lowering serum iron level in female beta thalassemia patients.
AbdulAzeez S; Almandil NB; Naserullah ZA; Al-Jarrash S; Al-Suliman AM; ElFakharay HI; Borgio JF
Mol Biol Rep; 2020 Jan; 47(1):603-606. PubMed ID: 31705350
[TBL] [Abstract][Full Text] [Related]
9. Two novel mutations in the 3' untranslated region of the beta-globin gene that are associated with the mild phenotype of beta thalassemia.
Bilgen T; Clark OA; Ozturk Z; Akif Yesilipek M; Keser I
Int J Lab Hematol; 2013 Feb; 35(1):26-30. PubMed ID: 22862814
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A Novel Mutation in the Promoter Region of the β-Globin Gene: HBB: c.-127G > C.
Bilgen T; Canatan D; Delibas S; Keser I
Hemoglobin; 2016 Aug; 40(4):280-2. PubMed ID: 27349616
[TBL] [Abstract][Full Text] [Related]
12. The Prevalence of
Saha J; Panja A; Nayek K
Hemoglobin; 2021 May; 45(3):157-162. PubMed ID: 34060430
[TBL] [Abstract][Full Text] [Related]
13. The effect of HBB: c.*+96T>C (3'UTR +1570 T>C) on the mild b-thalassemia intermedia phenotype.
Bilgen T; Canatan D; Arıkan Y; Yeşilipek A; Keser İ
Turk J Haematol; 2011 Sep; 28(3):219-22. PubMed ID: 27264370
[TBL] [Abstract][Full Text] [Related]
14. Severe Thalassemia Caused by Hb Zunyi [β147(HC3)Stop→Gln;
Su Q; Chen S; Wu L; Tian R; Yang X; Huang X; Chen Y; Peng Z; Chen J
Hemoglobin; 2019 Jan; 43(1):7-11. PubMed ID: 31084366
[TBL] [Abstract][Full Text] [Related]
15. Description of Three New α Variants and Four New β Variants: Hb Montluel [α110(G17)Ala → Val; HBA1: c.332C > T], Hb Cap d'Agde [α131(H14)Ser → Cys; HBA2: c.395C > G] and Hb Corsica [α100(G7)Leu → Pro; HBA1: 302T > C]; Hb Nîmes [β104(G6)Arg → Gly; HBB: c.313A > G], Hb Saint Marcellin [β112(G14)Cys → Gly; HBB: c.337T > G], Hb Saint Chamond [β80(EF4)Asn → 0; HBB: c.241_243delAAC] and Hb Dompierre [β29(B11)Gly → Arg; HBB: c.88G > C].
Renoux C; Feray C; Joly P; Lacan P; Francina A
Hemoglobin; 2015; 39(3):147-51. PubMed ID: 26100115
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A Cross-Sectional Study of Detection of Beta Globin (HBB) Haplotypes Among Beta Thalassemia Patients.
Alsamiri A; Alzahrani F; Filimban N; Khojah A; Felimban R; Qadah T
Cureus; 2021 Feb; 13(2):e13367. PubMed ID: 33754095
[TBL] [Abstract][Full Text] [Related]
18. The Spectrum of β-Thalassemia Mutations in Hamadan Province, West Iran.
Alibakhshi R; Moradi K; Aznab M; Azimi A; Shafieenia S; Biglari M
Hemoglobin; 2019 Jan; 43(1):18-22. PubMed ID: 31096791
[TBL] [Abstract][Full Text] [Related]
19. Prevalence and molecular characterization of structural hemoglobin variants in the Dongguan region of Guangdong province, southern China.
Lou JW; Wang T; Liu YH; He Y; Zhong BM; Liu JX; Zhao Y; Ye WL; Li DZ
Hemoglobin; 2014; 38(4):282-6. PubMed ID: 24985555
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
