118 related articles for article (PubMed ID: 38926992)
1. [Molecular Diagnosis and Pedigree Analysis of Rare Mutations in Non-coding Region of
Chen LZ; Yan TZ; Huang J; Zhong QY; Qin X; Tang N; Luo SQ
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2024 Jun; 32(3):940-944. PubMed ID: 38926992
[TBL] [Abstract][Full Text] [Related]
2. Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare α-Thalassemia Gene
Chen X; Luo S; Huang J; Yuan D; Yan T; Cai R; Tang N
Hemoglobin; 2020 Jan; 44(1):51-54. PubMed ID: 31933393
[TBL] [Abstract][Full Text] [Related]
3. [Cases Analysis of Hemoglobin H Disease Caused by
Wang QH; Chen XY; Tang N; Yan TZ; Huang J; Zhong QY; Luo SQ
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2024 Apr; 32(2):520-524. PubMed ID: 38660861
[TBL] [Abstract][Full Text] [Related]
4. Pedigree Analysis of Nonhomologous Sequence Recombination of
Luo SQ; Chen XY; Tang N; Huang J; Zhong QY; Cai R; Yan TZ
Hemoglobin; 2020 Sep; 44(5):329-333. PubMed ID: 32811243
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-Thalassemia.
Alauddin H; Kamarudin K; Loong TY; Azma RZ; Ithnin A; Jalil N; Razak NF; Koh-Xuan-Rong D; Ismail E; C-Khai L; Abdul Latiff Z; Alias H; Othman A
Hemoglobin; 2018 Jul; 42(4):247-251. PubMed ID: 30623696
[TBL] [Abstract][Full Text] [Related]
7. Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G).
Viprakasit V; Ekwattanakit S; Chalaow N; Riolueang S; Wijit S; Tanyut P; Chat-Uthai N; Tachavanich K
Acta Haematol; 2014; 131(2):88-94. PubMed ID: 24081251
[TBL] [Abstract][Full Text] [Related]
8. Two novel α2 gene mutations causing altered amino acid sequences produce a mild (Hb Kinshasa, HBA2: c.428A > T) and severe (HBA2: c.342-345insCC) α-thalassemia phenotype.
Saller E; Dutly F; Frischknecht H
Hemoglobin; 2015; 39(2):144-6. PubMed ID: 25786670
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Heterozygosity for the Novel
Forouzesh Pour F; Karimi K; Ghaderi Z; Tavakoli Koudehi A; Najmabadi H
Hemoglobin; 2020 Nov; 44(6):423-426. PubMed ID: 33054440
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. A Novel Mutation of the α2-Globin Gene Causing α
Chen B; Lin L; Yi S; Chen Q; Wei H; Li G; Zheng C; He S; Qiu X
Hemoglobin; 2017 Jan; 41(1):56-58. PubMed ID: 28395547
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Molecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (AT
Lei YL; Sui H; Liu YJ; Pan JJ; Liu YH; Lou JW
Hemoglobin; 2019; 43(4-5):241-244. PubMed ID: 31690131
[TBL] [Abstract][Full Text] [Related]
15. Hemoglobin profile and molecular characteristics of the complex interaction of hemoglobin Doi-Saket [α9(A7) asn > lys, HBA2:c.30C > a], a novel α2α1 hybrid globin variant, with hemoglobin E [β26(B8) Glu > lys, HBB:c.79G > A] and deletional α
Panyasai S; Khongthai K; Satthakarn S
Ann Med; 2023; 55(2):2264174. PubMed ID: 37796611
[TBL] [Abstract][Full Text] [Related]
16. First study to describe a novel
Yao C; Qin D; Wang J; Bao X; Liang J; Du L
Hematology; 2022 Dec; 27(1):867-873. PubMed ID: 35938954
[TBL] [Abstract][Full Text] [Related]
17. Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two α-Globin Gene Defects, Hb Taybe D
Assaf N; El Zibaoui R; Monsef C; Abi Nassif T; Abboud M; Yazbek S
Hemoglobin; 2024 Mar; 48(2):129-132. PubMed ID: 38626925
[TBL] [Abstract][Full Text] [Related]
18. Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare α- and β-Globin Gene Variants in Thalassemia Alleles in the Chinese Population.
Zhuang J; Chen C; Fu W; Wang Y; Zhuang Q; Lu Y; Xie T; Xu R; Zeng S; Jiang Y; Xie Y; Wang G
Arch Pathol Lab Med; 2023 Feb; 147(2):208-214. PubMed ID: 35639603
[TBL] [Abstract][Full Text] [Related]
19. Hb H Disease Caused by Multiple Mutations in the Polyadenylation Signal Site and - -
Zhang Q; Fan X; Xu M; Zhang Y; Xu H; Wen X; Zhou W
Hemoglobin; 2017 May; 41(3):189-192. PubMed ID: 28950779
[TBL] [Abstract][Full Text] [Related]
20. α-thalassemia trait caused by frameshift mutations in exon 2 of the α2-globin gene: HBA2:c.131delT and HBA2:c.143delA.
Finlayson J; Ghassemifar R; Holmes P; Grey D; Newbound C; Pell N; Jennens M; Greenwood L; Beilby J
Hemoglobin; 2012; 36(5):511-5. PubMed ID: 22943743
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
