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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 33559179)

  • 21. Beta-thalassemia and beta[A] globin gene haplotypes in Mexican mestizos.
    Villalobos-Arámbula AR; Bustos R; Casas-Castañeda M; Gutiérrez E; Perea FJ; Thein SL; Ibarra B
    Hum Genet; 1997 Apr; 99(4):498-500. PubMed ID: 9099840
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Characterization of a novel deletion causing (deltabeta)0-thalassemia in a Thai family.
    Svasti S; Paksua S; Nuchprayoon I; Winichagoon P; Fucharoen S
    Am J Hematol; 2007 Feb; 82(2):155-61. PubMed ID: 17034028
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Spectrum of beta thalassemia mutations and their linkage to beta-globin gene haplotypes in the Indo-Mauritians.
    Kotea N; Ramasawmy R; Lu CY; Fa NS; Gerard N; Beesoon S; Ducrocq R; Surrun SK; Nagel RL; Krishnamoorthy R
    Am J Hematol; 2000 Jan; 63(1):11-5. PubMed ID: 10602161
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal diagnosis of α- and β-thalassemias in southern Thailand.
    Nopparatana C; Nopparatana C; Saechan V; Karnchanaopas S; Srewaradachpisal K
    Int J Hematol; 2020 Feb; 111(2):284-292. PubMed ID: 31659625
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. β-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey.
    Guzelgul F; Seydel GS; Aksoy K
    Hemoglobin; 2020 Jul; 44(4):249-253. PubMed ID: 32664780
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The correlation of α-globin gene mutations and the XmnI polymorphism with clinical severity of Hb E/β-thalassemia.
    Charoenkwan P; Teerachaimahit P; Sanguansermsri T
    Hemoglobin; 2014; 38(5):335-8. PubMed ID: 25238043
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Description of a Rare β-Globin Gene Mutation: -86 (C>G) (HBB: c.-136C>G) Observed in a Syrian Family.
    Moassas F; Alabloog A; Murad H
    Hemoglobin; 2018 May; 42(3):203-205. PubMed ID: 30173596
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [The prevalence of beta-thalassemia heterozygotes compound alpha-thalassemia in Guangdong district].
    Han J; Zeng R; Hu B
    Zhonghua Xue Ye Xue Za Zhi; 2001 Oct; 22(10):514-6. PubMed ID: 11769674
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular basis of β-thalassemia in the United Arab Emirates.
    Baysal E
    Hemoglobin; 2011; 35(5-6):581-8. PubMed ID: 22074124
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Sudanese (δβ)0-Thalassemia: Identification and Characterization of a Novel 9.6 kb Deletion.
    Waye JS; Eng B; Got T; Hanna M; Hohenadel BA; Nakamura LM; Walker L
    Hemoglobin; 2015; 39(5):368-70. PubMed ID: 26154945
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Characterization of the 5' and 3' breakpoints of the Spanish (δβ)0-thalassemia deletion in Mexican patients.
    Guzmán LF; Perea FJ; Morales-González KR; Sánchez-López JY; de la Cruz EI; Chávez-Velasco ML; Ibarra CB
    Hemoglobin; 2011; 35(1):80-3. PubMed ID: 21250884
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Haplotype Analysis of Three Common β-Thalassemia Mutations in Syrian Patients.
    Murad H; Moassas F; Ghoury I; Mukhalalaty Y
    Hemoglobin; 2018; 42(5-6):302-305. PubMed ID: 30669902
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Analysis of beta-thalassemia mutations and beta-locus control region hypersensitive sites 2, 3 and 4 in southern Thailand.
    Sriroongrueng W; Schleiemacher E; Panich V; Nopparatana C; Saechan V; Laosombat V; Pornpatkul M; Fukumaki Y
    Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 3():120-7. PubMed ID: 9640613
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular heterogeneity of beta-thalassemia in Thailand.
    Fukumaki Y; Fucharoen S; Fucharoen G; Okamoto N; Ichinose M; Jetsrisuparb A; Sriroongrueng W; Nopparatana C; Laosombat V; Panich V
    Southeast Asian J Trop Med Public Health; 1992; 23 Suppl 2():14-21. PubMed ID: 1363706
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular basis of beta-thalassemia in Morocco: possible origins of the molecular heterogeneity.
    Agouti I; Badens C; Abouyoub A; Levy N; Bennani M
    Genet Test; 2008 Dec; 12(4):563-8. PubMed ID: 18976160
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A single-tube multiplex gap-polymerase chain reaction for the detection of eight β-globin gene cluster deletions common in Southeast Asia.
    Tritipsombut J; Phylipsen M; Viprakasit V; Chalaow N; Sanchaisuriya K; Giordano PC; Fucharoen S; Harteveld CL
    Hemoglobin; 2012; 36(6):571-80. PubMed ID: 23181748
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular Characterization of β-Thalassemia Intermedia in Southeast Iran.
    Miri-Moghaddam E; Bahrami S; Naderi M; Bazi A; Karimipoor M
    Hemoglobin; 2016 Jun; 40(3):173-8. PubMed ID: 27117567
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A Novel 5 kb Deletion in the
    Bao XQ; Wang JC; Qin DQ; Yao CZ; Liang J; Du L
    Hemoglobin; 2022 Jul; 46(4):245-248. PubMed ID: 36210651
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.