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 *

199 related articles for article (PubMed ID: 19420802)

  • 41. Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients.
    Qin D; Du L; Wang J; Yao C; Guo H; Yuan T; Liang J; Yin A
    J Int Med Res; 2020 Nov; 48(11):300060520967825. PubMed ID: 33213249
    [TBL] [Abstract][Full Text] [Related]  

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

  • 43. [Study on the screening program of thalassemia and the genotype and hematologic parameter among people of productive age in a village, Nanning Guangxi].
    Zhang XH; Zhou YJ; Li PP; Luo RG; Ruan LM; Wang RX; Wu ZK; Li M; Huang YW
    Zhonghua Liu Xing Bing Xue Za Zhi; 2006 Sep; 27(9):769-72. PubMed ID: 17299961
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Interaction of hemoglobin E and several forms of alpha-thalassemia in Cambodian families.
    Fucharoen S; Sanchaisuriya K; Fucharoen G; Panyasai S; Devenish R; Luy L
    Haematologica; 2003 Oct; 88(10):1092-8. PubMed ID: 14555303
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Study of the genotypic and hematological feature of hemoglobin H disease in West Guangxi area].
    Nong X; Xu G; Li J; Liang J; Zhong S; Liu C; Wang C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Dec; 37(12):1326-1330. PubMed ID: 33306814
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Adult onset of a Thalassemia intermedia genotype in association with a -alpha-3.7 homozygosity. Hb G-Accra [beta73(e17)Asp-->Asn] in combination with beta- and alpha-thalassemia in the same family.
    van der Padt A; Bouva M; Auwerda JJ; Dees A; Harteveld CL; Giordano PC
    Hemoglobin; 2005; 29(4):269-76. PubMed ID: 16370487
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (
    Nuinoon M; Thipthara O; Fucharoen S
    Hemoglobin; 2019 Jan; 43(1):52-55. PubMed ID: 31106603
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [Analysis of Gene Deficiency Types of Thalassemia in Lingui District of Guilin City].
    Xiang XH; Leng J; Wang D; Mo LJ; Jiang W; Wei CD
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2021 Jun; 29(3):860-864. PubMed ID: 34105484
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Distribution of thalassemias and associated hemoglobinopathies identified by prenatal diagnosis in Taiwan.
    Peng CT; Liu SC; Peng YC; Lin TH; Wang SJ; Le CY; Shih MC; Tien N; Lu JJ; Lin CY
    Blood Cells Mol Dis; 2013 Oct; 51(3):138-41. PubMed ID: 23689197
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Mild hemoglobin H-constant spring disease with β-thalassemia-a case report.
    Li DZ; Liao C; Zhou JY; Xie XM; Li J
    Ann Hematol; 2011 Jan; 90(1):123-4. PubMed ID: 20383502
    [No Abstract]   [Full Text] [Related]  

  • 51. [Genotypes and clinical features of 595 children with HbH disease in Guangxi, China].
    He S; Zhang Q; Chen BY; Huang P; Tang YQ; Wei Y; Chen QL; Zheng CG
    Zhongguo Dang Dai Er Ke Za Zhi; 2015 Sep; 17(9):908-11. PubMed ID: 26412168
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Co-inheritance of α-thalassaemia and β-thalassaemia in a prenatal screening population in mainland China.
    Li J; Xie XM; Liao C; Li DZ
    J Med Screen; 2014 Dec; 21(4):167-71. PubMed ID: 25118159
    [TBL] [Abstract][Full Text] [Related]  

  • 53. 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]  

  • 54. beta-thalassemia intermedia caused by compound heterozygosity for Hb Malay (beta codon 19 AAC-->AGC; asn-->Ser) and codons 41/42 (-CTTT) beta(0)-thalassemia mutation.
    Ma SK; Chow EY; Chan AY; Kung NN; Waye JS; Chan LC; Chui DH
    Am J Hematol; 2000 Jul; 64(3):206-9. PubMed ID: 10861818
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. [Genetic Diagnosis of Thalassemia in Baise, Guangxi Zhuang Autonomous Region].
    Lu H; Qin Q; Li JH; Chen T; Liang SJ; Lu XS
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2021 Jun; 29(3):865-868. PubMed ID: 34105485
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Genotype analysis of 55,281 cases of thalassemia in northern Guangxi.
    Zeng D; Chen Z; Yang Y; Li J; Tian B; Mo L
    Am J Transl Res; 2024; 16(1):51-62. PubMed ID: 38322564
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Analysis of hematological phenotype and genotype of 23 patients from Guangdong with co-inherited hemoglobin Hb Westmead and β-thalassemia].
    Yan M; Gan X; Liu M; Huang B; Zhong L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):598-601. PubMed ID: 27577202
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Genetic origin of α
    Jomoui W; Fucharoen G; Sanchaisuriya K; Charoenwijitkul P; Maneesarn J; Xu X; Fucharoen S
    J Hum Genet; 2017 Aug; 62(8):747-754. PubMed ID: 28381876
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Genetic determinants of β-thalassemia intermedia in Pakistan.
    Khan J; Ahmad N; Siraj S; Hoti N
    Hemoglobin; 2015; 39(2):95-101. PubMed ID: 25707679
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.