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 *

157 related articles for article (PubMed ID: 36900038)

  • 1. Gene Mutation Spectrum among Alpha-Thalassaemia Patients in Northeast Peninsular Malaysia.
    Vijian D; Wan Ab Rahman WS; Ponnuraj KT; Zulkafli Z; Bahar R; Yasin N; Hassan S; Esa E
    Diagnostics (Basel); 2023 Feb; 13(5):. PubMed ID: 36900038
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hematological Profile of Hb Adana Among High School Students in Northeast Peninsular Malaysia.
    Siti Asmaa MJ; Miin Phoon L; Zakaria NA; Hussin S; Bahar R; Hassan MN; Zulkafli Z; Iberahim S; Abdullah M; Mohd Noor NH; Mohamed Yusoff S; Ramli M
    Cureus; 2024 Mar; 16(3):e57353. PubMed ID: 38694420
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular characteristic of alpha thalassaemia among patients diagnosed in UKM Medical Centre.
    Azma RZ; Ainoon O; Hafiza A; Azlin I; Noor Farisah AR; Nor Hidayati S; Noor Hamidah H
    Malays J Pathol; 2014 Apr; 36(1):27-32. PubMed ID: 24763232
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular Study of Deletional and Nondeletional Mutations on the α-Globin Locus in the Azeri Population of Northwestern Iran.
    Derakhshan SM; Khaniani MS; Afkhami F; PourFeizi AH
    Hemoglobin; 2016 Sep; 40(5):319-322. PubMed ID: 27690152
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and haematological characteristics of 38 individuals with Hb G-Makassar in Malaysia.
    Esa E; Mohamad AS; Hamzah R; Hamid FSA; Aziz NA; Sevaratnam V; Sathar J; Chen G; Yasin NM
    EJHaem; 2023 Nov; 4(4):940-948. PubMed ID: 38024609
    [TBL] [Abstract][Full Text] [Related]  

  • 6. DNA studies are necessary for accurate patient diagnosis in compound heterozygosity for Hb Adana (HBA2:c.179>A) with deletional or nondeletional α-thalassaemia.
    Tan JAMA; Kho SL; Ngim CF; Chua KH; Goh AS; Yeoh SL; George E
    Sci Rep; 2016 Jun; 6():26994. PubMed ID: 27271331
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular characterisation of Haemoglobin Constant Spring and Haemoglobin Quong Sze with a Combine-Amplification Refractory Mutation System.
    Wee YC; Tan KL; Chua KH; George E; Tan JA
    Malays J Med Sci; 2009 Jul; 16(3):21-8. PubMed ID: 22589661
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical experience using peripheral blood parameters to analyse the mutation type of thalassemia carriers in pregnant women.
    Zhu S; Yin J; Luo Y; Chen Y; Lin Z; Fu X; Li H; Su H
    J Obstet Gynaecol; 2023 Dec; 43(1):2195490. PubMed ID: 37038923
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Analysis of the Types of Thalassemia Gene Mutations in Nanping Area of Fujian, China].
    Chen MF; Huang MZ; Lin Q; Huang J; Chen F; Zhang JY; Xue F
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2020 Jun; 28(3):918-926. PubMed ID: 32552958
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High-resolution melting analysis of the three common nondeletional α-thalassemia mutations in the Chinese population: Hbs Constant Spring, Quong Sze and Westmead.
    Li R; Liao C; Li D; Li J
    Hemoglobin; 2010; 34(6):587-93. PubMed ID: 21077768
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic basis of persistent red blood cell microcytosis in the Chinese unexplained by phenotypical testing.
    So CC; Liu AK; Tsang MH; Ngai DY; Leung KS; Chan AY
    J Clin Pathol; 2015 Jan; 68(1):69-72. PubMed ID: 25352644
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A laboratory strategy for genotyping haemoglobin H disease in the Chinese.
    Chan AY; So CC; Ma ES; Chan LC
    J Clin Pathol; 2007 Aug; 60(8):931-4. PubMed ID: 17018682
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of α1 and α2 globin genes among patients with hemoglobin Adana in Malaysia.
    Lee TY; Lai MI; Ismail P; Ramachandran V; Tan JA; Teh LK; Othman R; Hussein NH; George E
    Genet Mol Res; 2016 Apr; 15(2):. PubMed ID: 27173219
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The spectrum of α-thalassemia mutations in the Kurdish population of Northeastern Iraq.
    Al-Allawi NA; Jalal SD; Rasheed NS; Bayat N; Imanian H; Najmabadi H; Faraj A
    Hemoglobin; 2013; 37(1):56-64. PubMed ID: 23215864
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of α-thalassaemia in neonates on cord blood and dried blood spot samples by capillary electrophoresis.
    Alauddin H; Langa M; Mohd Yusoff M; Raja Sabudin RZA; Ithnin A; Abdul Razak NF; Sardi NH; Hussin NH
    Malays J Pathol; 2017 Apr; 39(1):17-23. PubMed ID: 28413201
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Effects of α-thalassaemia mutations on the haematological parameters of β-thalassaemia carriers.
    Saleh-Gohari N; Khademi Bami M; Nikbakht R; Karimi-Maleh H
    J Clin Pathol; 2015 Jul; 68(7):562-6. PubMed ID: 25935548
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular Characterisation of α- and β-Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia.
    Koh DXR; Raja Sabudin RZA; Mohd Yusoff M; Hussin NH; Ahmad R; Othman A; Ismail E
    Ann Hum Genet; 2017 Sep; 81(5):205-212. PubMed ID: 28620953
    [TBL] [Abstract][Full Text] [Related]  

  • 18. First report of the spectrum of δ-globin gene mutations among women of reproductive age in Fujian area-Discrimination of δ-thalassemia, α-thalassemia, and Iron Deficiency Anemia.
    Chen M; Huang H; Chen L; Lin N; Zhang M; Lin Y; Xu L
    J Clin Lab Anal; 2020 Nov; 34(11):e23479. PubMed ID: 32901995
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pedigree Analysis of Nonhomologous Sequence Recombination of
    Luo SQ; Chen XY; Tang N; Huang J; Zhong QY; Cai R; Yan TZ
    Hemoglobin; 2020 Sep; 44(5):329-333. PubMed ID: 32811243
    [TBL] [Abstract][Full Text] [Related]  

  • 20. HbA2 levels in β-thalassaemia carriers with the Filipino β0-deletion: are the levels higher than what is found with non-deletional forms of β0-thalassaemia?
    George E; Teh LK; Tan J; Lai MI; Wong L
    Pathology; 2013 Jan; 45(1):62-5. PubMed ID: 23222244
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.