These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
196 related articles for article (PubMed ID: 37309066)
1. 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]
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. 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]
4. 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]
5. Elevated Hb A₂ Levels in a Patient with a Compound Heterozygosity for the (β⁺) -31 (A > G) and (β⁰) Codon 17 (A > T) Mutations Together with a Single α-Globin Gene. Panyasai S; Jaiping K; Pornprasert S Hemoglobin; 2015; 39(4):292-5. PubMed ID: 26029792 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Profiling of 35 Cases of Hb S/Hb E ( Dehury S; Mohanty PK; Patel S; Meher S; Das K; Purohit P; Sahoo S; Ratha J Hemoglobin; 2021 Nov; 45(6):380-386. PubMed ID: 35243949 [TBL] [Abstract][Full Text] [Related]
8. First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family. Murad H; Moassas F Hemoglobin; 2019 Jan; 43(1):66-68. PubMed ID: 30843739 [TBL] [Abstract][Full Text] [Related]
9. The phenomena of balanced effect between α-globin gene and of β-globin gene. Zhong L; Gan X; Xu L; Liang C; Xie Y; Lin W; Chen P; Liu M BMC Med Genet; 2018 Aug; 19(1):145. PubMed ID: 30119651 [TBL] [Abstract][Full Text] [Related]
10. [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]
11. 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]
12. Double Heterozygosity for Hb Durham-N.C. ( Cannata M; Cassarà F; Vinciguerra M; Licari P; Passarello C; Leto F; Lo Pinto C; Pitrolo L; Ganci R; Maggio A; Giambona A Hemoglobin; 2019 May; 43(3):210-213. PubMed ID: 31456457 [TBL] [Abstract][Full Text] [Related]