504 related articles for article (PubMed ID: 32885601)
1. 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]
2. 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]
3. [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]
4. 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]
5. Detection of a Hb A
Li Y; Huang T; Mao T; Zhang X; Liang L; Meng M
J Clin Lab Anal; 2020 Sep; 34(9):e23401. PubMed ID: 32770585
[TBL] [Abstract][Full Text] [Related]
6. Association of Hb A
Panyasai S; Pornprasert S
Hemoglobin; 2020 May; 44(3):179-183. PubMed ID: 32482156
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [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]
9. [A rare thalassemia intermedia case caused by co-existence of Hb H disease (--(SEA)/-alpha(4.2)) and beta-thalassemia major (beta (CD17A)>T/beta (IVS2-654C)>T): implications for prenatal diagnosis].
Li Q; Li LY; Mo QH
Nan Fang Yi Ke Da Xue Xue Bao; 2008 Jan; 28(1):16-9. PubMed ID: 18227017
[TBL] [Abstract][Full Text] [Related]
10. [Analysis of the Types of Thalassemia Gene Mutations in Nanping Area of Fujian, China].
Chen MF; Huang MZ; Lin Q; Huang J; Chen F; Zhang JY; Xue F
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2020 Jun; 28(3):918-926. PubMed ID: 32552958
[TBL] [Abstract][Full Text] [Related]
11. Hb Athens-Georgia (beta 40(C6) Arg > Lys, HBB:c.122G > A) with a single α-globin gene (Hb H disease) in a Thai family: molecular, hematological, and diagnostic aspects.
Panyasai S; Kunyanone N; Satthakarn S
Scand J Clin Lab Invest; 2021 Feb; 81(1):52-58. PubMed ID: 33287582
[TBL] [Abstract][Full Text] [Related]
12. Analysis of Hb levels and degree of anemia in relation to genotype in 615 patients with hemoglobin H disease.
Luo S; Chen X; Chen L; Zhong Q; Wang Q; Xu Z; Huang J; Yan T; Tang N
Expert Rev Hematol; 2020 Sep; 13(9):1027-1033. PubMed ID: 32727230
[TBL] [Abstract][Full Text] [Related]
13. Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare β-Globin Mutations.
Qiu Y; Wei S; Hou W; Lai K; Zhu H; Li W; Li Q; Yang Z; Shu Q; Chen P; Mo W
Hemoglobin; 2023 Nov; 47(2):52-55. PubMed ID: 37309066
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Analysis of Gene Mutation Types of α- and β-Thalassemia in Fuzhou, Fujian Province in China.
Xu C; Liao B; Qi Y; Huangfu Z; Chen J; Chen Y
Hemoglobin; 2018 May; 42(3):143-147. PubMed ID: 30348032
[TBL] [Abstract][Full Text] [Related]
16. [Characteristics of Silent Alpha Thalassemia Gene in Child-Bearing Adults in Guangdong].
Huang G; Zheng YW; Wu J; Liu SN
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2023 Dec; 31(6):1811-1814. PubMed ID: 38071065
[TBL] [Abstract][Full Text] [Related]
17. Hb H disease with various β hemoglobinopathies: molecular, hematological and diagnostic aspects.
Fucharoen S; Fucharoen G
Hemoglobin; 2012; 36(1):18-24. PubMed ID: 22145566
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Analysis of rare thalassemia caused by HS-40 regulatory site deletion.
Luo S; Chen X; Zhong Q; Wang Q; Xu Z; Qin L; Wang J; Yuan D; Yan T; Tang N
Hematology; 2020 Dec; 25(1):286-291. PubMed ID: 32720864
[No Abstract] [Full Text] [Related]
20. Prenatal Diagnosis and Screening of Thalassemia Mutations in Bangladesh: Presence of Rare Mutations.
Aziz MA; Khan WA; Banu B; Das SA; Sadiya S; Begum S
Hemoglobin; 2020 Nov; 44(6):397-401. PubMed ID: 33092414
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]