BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 15182058)

  • 21. First Case of a Compound Heterozygosity for Two Nondeletional α-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze.
    Zhou JY; Yan JM; Li J; Li DZ
    Hemoglobin; 2016 Jun; 40(3):210-2. PubMed ID: 26956449
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Evaluation of Alpha-Thalassemia Mutations in Cases with Hypochromic Microcytic Anemia: The İstanbul Perspective.
    Karakaş Z; Koç B; Temurhan S; Elgün T; Karaman S; Asker G; Gençay G; Timur Ç; Yıldırmak ZY; Celkan T; Devecioğlu Ö; Aydın F
    Turk J Haematol; 2015 Dec; 32(4):344-50. PubMed ID: 26377141
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease.
    Viprakasit V; Tanphaichitr VS; Veerakul G; Chinchang W; Petrarat S; Pung-Amritt P; Higgs DR
    Am J Hematol; 2004 Mar; 75(3):157-63. PubMed ID: 14978697
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Detection of Hb Constant Spring [α142, Term→Gln, TAA>CAA (α2)] in heterozygotes combined with β-thalassemia.
    Li YQ; Li R; Li DZ
    Hemoglobin; 2013; 37(2):197-200. PubMed ID: 23390935
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The alpha / beta and alpha 2 / alpha 1-globin mRNA ratios in different forms of alpha-thalassemia.
    Smetanina NS; Leonova JY; Levy N; Huisman TH
    Biochim Biophys Acta; 1996 Apr; 1315(3):188-92. PubMed ID: 8611658
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Complex interaction of Hb E [beta26(B8)Glu-->Lys], Hb Korle-Bu [beta73(E17)Asp-->Asn] and a deletional alpha-thalassemia-1 in pregnancy.
    Siriratmanawong N; Chansri W; Singsanan S; Fucharoen G; Fucharoen S
    Hemoglobin; 2009; 33(6):507-14. PubMed ID: 19958198
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Application of Next Generation Sequencing to Screen the Neonatal Thalassemia Genes].
    Tan M; Lu S; Wu LS; Jin DW; Peng ZY; Chen Y
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2015 Oct; 23(5):1404-9. PubMed ID: 26524047
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Association of Hb A
    Panyasai S; Pornprasert S
    Hemoglobin; 2020 May; 44(3):179-183. PubMed ID: 32482156
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in India.
    Colah R; Nadkarni A; Gorakshakar A; Phanasgaonkar S; Surve R; Subramaniam PG; Bondge N; Pujari K; Ghosh K; Mohanty D
    Blood Cells Mol Dis; 2004; 33(2):153-7. PubMed ID: 15315795
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. [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]  

  • 33. Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation.
    Singh SA; Sarangi S; Appiah-Kubi A; Hsu P; Smith WB; Gallagher PG; Glader B; Chui DHK
    Pediatr Blood Cancer; 2018 Sep; 65(9):e27220. PubMed ID: 29749692
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Alpha 2 codon 30 deletion (deltaGAG) causing non-deletional hemoglobin H disease in Guangxi province].
    Chen P; Li SQ; Wu H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):435-9. PubMed ID: 15476164
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Co-inheritance of alpha-and beta-thalassemia in Khuzestan Province, Iran.
    Rahim F; Kaikhaei B; Zandian K; Hoseini A
    Hematology; 2008 Feb; 13(1):59-64. PubMed ID: 18534068
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular pathogenesis and clinical variability of homozygous beta0-thalassemia in populations of Jammu region of J&K state (India).
    Singh SP; Gupta S
    Hematology; 2006 Aug; 11(4):271-5. PubMed ID: 17178667
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Complex interaction of Hb Hekinan [alpha27(B8) Glu-Asp] and Hb E [beta26(B8) Glu-Lys] with a deletional alpha-thalassemia 1 in a Thai family.
    Fucharoen S; Changtrakun Y; Ratanasiri T; Fucharoen G; Sanchaisuriya K
    Eur J Haematol; 2003 May; 70(5):304-9. PubMed ID: 12694166
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.
    Azma RZ; Othman A; Azman N; Alauddin H; Ithnin A; Yusof N; Razak NF; Sardi NH; Hussin NH
    Malays J Pathol; 2012 Jun; 34(1):57-62. PubMed ID: 22870600
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Novel interactions of two α-Hb variants with SEA deletion α
    Srivorakun H; Singha K; Fucharoen G; Fucharoen S
    Hematology; 2018 Apr; 23(3):187-191. PubMed ID: 28945175
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 11.