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Journal Abstract Search

544 related items for PubMed ID: 26377141

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  • 3. Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common alpha-thalassemia point mutations and deletions.
    Puehringer H, Najmabadi H, Law HY, Krugluger W, Viprakasit V, Pissard S, Baysal E, Taher A, Farra C, Al-Ali A, Al-Ateeq S, Oberkanins C.
    Clin Chem Lab Med; 2007; 45(5):605-10. PubMed ID: 17484620
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  • 4. The Hematological and Molecular Spectrum of α-Thalassemias in Turkey: The Hacettepe Experience.
    Ünal Ş, Gümrük F.
    Turk J Haematol; 2015 Jun; 32(2):136-43. PubMed ID: 26316481
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  • 5. A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease.
    Farashi S, Faramarzi Garous N, Zeinali F, Vakili S, Ashki M, Imanian H, Najmabadi H, Azarkeivan A, Tamaddoni A.
    Hemoglobin; 2015 Jun; 39(3):196-200. PubMed ID: 25976776
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  • 7. Molecular analysis of complex cases of alpha- and beta-thalassemia in Mexican mestizo patients with microcytosis and hypochromia reveals two novel alpha(0) -thalassemia deletions - -(Mex1) and - -(Mex2).
    de-la-Cruz-Salcedo EI, Ibarra B, Rizo-de-la-Torre LC, Sánchez-López JY, González-Mercado A, Harteveld CL, Perea-Díaz FJ.
    Int J Lab Hematol; 2016 Oct; 38(5):535-42. PubMed ID: 27339814
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  • 8. Mutations on the α2-Globin Gene That May Trigger α(+)-Thalassemia.
    Farashi S, Vakili S, Garous NF, Ashki M, Imanian H, Azarkeivan A, Najmabadi H.
    Hemoglobin; 2015 Oct; 39(6):398-402. PubMed ID: 26329872
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  • 9. α-Thalassemia frequency and mutations in children with hypochromic microcytic anemias and relation with β-thalassemia, iron deficiency anemia.
    Gulen H, Hanimeli O, Karaca O, Taneli F.
    Pediatr Hematol Oncol; 2012 Apr; 29(3):241-6. PubMed ID: 22475300
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  • 10. Alpha-globin gene mutation spectrum in patients with microcytic hypochromic anemia from Mazandaran Province, Iran.
    Hashemi-Soteh SMB, Karami H, Mousavi SS, Farazmandfar T, Tamadoni A.
    J Clin Lab Anal; 2020 Jan; 34(1):e23018. PubMed ID: 31478238
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  • 11. Analysis of rare thalassemia caused by HS-40 regulatory site deletion.
    Luo S, Chen X, Zhong Q, Wang Q, Xu Z, Qin L, Wang J, Yuan D, Yan T, Tang N.
    Hematology; 2020 Dec; 25(1):286-291. PubMed ID: 32720864
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  • 12. Molecular spectrum of alpha-thalassemia mutations in microcytic hypochromic anemia patients from Saudi Arabia.
    Hellani A, Fadel E, El-Sadadi S, El-Sweilam H, El-Dawood A, Abu-Amero KK.
    Genet Test Mol Biomarkers; 2009 Apr; 13(2):219-21. PubMed ID: 19371220
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  • 13. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
    Zhu BS, He J, Zhang J, Zeng XH, Su J, Xu XH, Li SY, Chen H, Zhang YH.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
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  • 14. Uncommon Combination of Hemoglobin Jax and Hemoglobin Constant Spring Leading to Microcytic Anemia.
    Srichairatanakool S, Chai-Adisaksopha C, Tantiworawit A, Phusua A, Charoenkwan P.
    Am J Case Rep; 2024 May 10; 25():e943560. PubMed ID: 38725231
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  • 15. Alpha-thalassemia mutations in Gilan Province, North Iran.
    Hadavi V, Jafroodi M, Hafezi-Nejad N, Moghadam SD, Eskandari F, Tarashohi S, Pourfahim H, Oberkanins C, Law HY, Najmabadi H.
    Hemoglobin; 2009 May 10; 33(3):235-41. PubMed ID: 19657838
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  • 16. α-Thalassemia mutations in two provinces of Southern Iran: Fars & Kohkeloye and Bouyer Ahmad.
    Hossein F, Mohsen R, Mohsen M, Taheri M.
    Hemoglobin; 2012 May 10; 36(2):139-43. PubMed ID: 22401170
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  • 17. α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region.
    Al-Riyami AZ, Daar S, Kindi SA, Madhani AA, Wali Y, Rawahi MA, Zadjali SA.
    Hemoglobin; 2020 Jan 10; 44(1):20-26. PubMed ID: 32019385
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  • 19. Alpha-thalassemia phenotype induced by the new IVS-II-2 (T --> A) splice donor site mutation on the alpha2-globin gene.
    Harteveld CL, Jebbink MC, van der Lely N, van Delft P, Akkermans N, Arkesteyn S, Giordano PC.
    Hemoglobin; 2006 Jan 10; 30(1):3-7. PubMed ID: 16540408
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  • 20. A Novel Mutation of the α2-Globin Gene Causing α+-Thalassemia: Hb Nanning (HBA2: c.369_370delinsGA).
    Chen B, Lin L, Yi S, Chen Q, Wei H, Li G, Zheng C, He S, Qiu X.
    Hemoglobin; 2017 Jan 10; 41(1):56-58. PubMed ID: 28395547
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