137 related articles for article (PubMed ID: 29722583)
21. Mutational spectrum of HBD gene in the Chinese population: Description of 36 mutations including 11 novel variants.
Xu A; Li M; Ye Y; Li L; Ma M; Wu SY; Ji L
Int J Lab Hematol; 2023 Dec; 45(6):961-968. PubMed ID: 37605839
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Hb A2-Konz [δ50(D1)Ser → Thr; HBD: c.151T > A]: a new δ chain hemoglobin variant characterized by mass spectrometry and high performance liquid chromatography.
Alayi TD; Van Dorsselaer A; Epting T; Bissé E; Schaeffer-Reiss C
Hemoglobin; 2014; 38(2):133-6. PubMed ID: 24471805
[TBL] [Abstract][Full Text] [Related]
24. Hb A
Lederer CW; Pavlou E; Tanteles GA; Evangelidou P; Sismani C; Kolnagou A; Sitarou M; Christou S; Hadjigavriel M; Kleanthous M
Hematology; 2017 Jun; 22(5):304-309. PubMed ID: 28007020
[TBL] [Abstract][Full Text] [Related]
25. Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations.
Kasmi C; Amri Y; Hadj-Fredj S; Oueslati S; Dabboussi M; Mahjoub R; Hammami S; Aljane I; Mami FB; Jamoussi H; Messaoud T; Bibi A
Mol Biol Rep; 2021 Aug; 48(8):5923-5933. PubMed ID: 34341901
[TBL] [Abstract][Full Text] [Related]
26. A New δ-Globin Gene Variant: Hb A2-Yulin [δ46(CD5)Gly→Arg,
Lin HM; Liang L; Cai YJ; Zheng LH; Qin QP; Li YQ
Hemoglobin; 2024 Mar; 48(2):121-124. PubMed ID: 38450437
[TBL] [Abstract][Full Text] [Related]
27. Analysis of δ-globin gene mutations in the Chinese population.
Liu N; Xie XM; Zhou JY; Li R; Liao C; Li DZ
Hemoglobin; 2013; 37(1):85-93. PubMed ID: 23215833
[TBL] [Abstract][Full Text] [Related]
28. Development of a High Resolution Melting Curve Analysis for the Detection of Hemoglobin δ-Chain Variants in Thailand and Identification of Hb A2-Walsgrave [codon 52 (GAT>CAT), Asp→His; HBD:c.157G>C] in a Pregnant Woman from Southern Thailand.
Prajantasen T; Prayalaw P; Panyasai S; Binlee S; Nongnuan S
Genet Test Mol Biomarkers; 2021 Jun; 25(6):426-433. PubMed ID: 34152843
[No Abstract] [Full Text] [Related]
29. A Woman with Missing Hb A
Saller E; Knijnenburg J; Harteveld CL; Dutly F
Hemoglobin; 2020 May; 44(3):214-217. PubMed ID: 32605393
[TBL] [Abstract][Full Text] [Related]
30. Association of Hb A
Panyasai S; Pornprasert S
Hemoglobin; 2020 May; 44(3):179-183. PubMed ID: 32482156
[TBL] [Abstract][Full Text] [Related]
31. First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in Iran.
Amirian A; Karimipoor M; Jafarinejad M; Taghavi M; Kordafshari A; Fathi Azar S; Mohammadi MS; Zeinali S
Arch Iran Med; 2011 Jan; 14(1):8-11. PubMed ID: 21194254
[TBL] [Abstract][Full Text] [Related]
32. Genotype-phenotype relationship of the δ-thalassemia and Hb A(2) variants: observation of 52 genotypes.
Lacerra G; Scarano C; Lagona LF; Testa R; Caruso DG; Medulla E; Friscia MG; Mastrullo L; Caldora M; Prezioso R; Gaudiano C; Magnano C; Romeo MA; Musollino G; Di Noce F; Carestia C
Hemoglobin; 2010; 34(5):407-23. PubMed ID: 20854114
[TBL] [Abstract][Full Text] [Related]
33. Hb A
Chen GL; Huang LY; Zhou JY; Li DZ
Hemoglobin; 2017; 41(4-6):291-292. PubMed ID: 29251016
[TBL] [Abstract][Full Text] [Related]
34. First description of a Hb A2 variant in Thailand. Identification of Hb A2-Melbourne [δ43(CD2)Glu→Lys] in Thai individuals.
Chaibunruang A; Fucharoen G; Fucharoen S
Hemoglobin; 2012; 36(1):80-4. PubMed ID: 21967556
[TBL] [Abstract][Full Text] [Related]
35. Prospective screening for δ-hemoglobinopathies associated with decreased hemoglobin A
Hanart C; Singha K; Changtrakul Y; Fucharoen S; Srivorakun H
Clin Chim Acta; 2023 Jul; 547():117417. PubMed ID: 37276945
[TBL] [Abstract][Full Text] [Related]
36. δ-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia.
Singha K; Fucharoen G; Fucharoen S
Ann Hematol; 2021 Aug; 100(8):1953-1963. PubMed ID: 33834283
[TBL] [Abstract][Full Text] [Related]
37. A novel δ-globin gene mutation (HBD: c.323G>A) masking the diagnosis of β-thalassemia: a first report from India.
Jain S; Edison ES; Mathews V; Shaji RV
Int J Hematol; 2012 May; 95(5):570-2. PubMed ID: 22477537
[TBL] [Abstract][Full Text] [Related]
38. Characterization of three novel delta chain hemoglobin variants and two delta-thalassemia alleles.
Frischknecht H; Troxler H; Dutly F; Walker L; Hohenadel BA; Eng B; Waye JS
Hemoglobin; 2010; 34(4):374-82. PubMed ID: 20642335
[TBL] [Abstract][Full Text] [Related]
39. Co-inheritance of β- and δ-thalassemia compromising prenatal screening in a Chinese couple seeking prevention.
Li J; Xie XM; Zhou JY; Li DZ
Fetal Diagn Ther; 2011; 30(1):73-6. PubMed ID: 21494010
[TBL] [Abstract][Full Text] [Related]
40. Two new δ-globin gene variants: Hb A(2)-Saint-Etienne [δ14(A11)Leu→Pro (HBD: c.44T>C)] and Hb A(2)-Marseille [δ22(B4) Ala→Lys (HBD: c.67G>A;68C>A)].
Joly P; Lacan P; Garcia C; Desbrée A; Couprie N; Francina A
Hemoglobin; 2013; 37(1):80-4. PubMed ID: 23227922
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]