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Journal Abstract Search

323 related items for PubMed ID: 27173810

  • 1. Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism.
    Fu C, Xie B, Zhang S, Wang J, Luo S, Zheng H, Su J, Hu X, Chen R, Fan X, Luo J, Gu X, Chen S.
    BMJ Open; 2016 May 12; 6(5):e010719. PubMed ID: 27173810
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  • 2. Mutation screening of DUOX2 in Chinese patients with congenital hypothyroidism.
    Fu C, Zhang S, Su J, Luo S, Zheng H, Wang J, Qin H, Chen Y, Shen Y, Hu X, Fan X, Luo J, Xie B, Chen R, Chen S.
    J Endocrinol Invest; 2015 Nov 12; 38(11):1219-24. PubMed ID: 26349762
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  • 3. Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patients.
    Fu C, Luo S, Zhang S, Wang J, Zheng H, Yang Q, Xie B, Hu X, Fan X, Luo J, Chen R, Su J, Shen Y, Gu X, Chen S.
    Clin Chim Acta; 2016 Jul 01; 458():30-4. PubMed ID: 27108200
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  • 4. Compound heterozygous mutations (p.T561M and c.2422delT) in the TPO gene associated with congenital hypothyroidism.
    Ma SG, Zheng X, Qiu YL, Guo ML, Shao XJ.
    J Pediatr Endocrinol Metab; 2016 May 01; 29(5):567-70. PubMed ID: 27135621
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  • 7. Genotypes and phenotypes of congenital goitre and hypothyroidism caused by mutations in dual oxidase 2 genes.
    Wang F, Lu K, Yang Z, Zhang S, Lu W, Zhang L, Liu S, Yan S.
    Clin Endocrinol (Oxf); 2014 Sep 01; 81(3):452-7. PubMed ID: 24735383
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  • 8. Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients.
    Fu C, Wang J, Luo S, Yang Q, Li Q, Zheng H, Hu X, Su J, Zhang S, Chen R, Luo J, Zhang Y, Shen Y, Wei H, Meng D, Gui B, Zeng Z, Fan X, Chen S.
    Clin Chim Acta; 2016 Nov 01; 462():127-132. PubMed ID: 27637299
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  • 9. Newborn screening and single nucleotide variation profiling of TSHR, TPO, TG and DUOX2 candidate genes for congenital hypothyroidism.
    Kollati Y, Akella RRD, Naushad SM, Borkar D, Thalla M, Nagalingam S, Lingappa L, Patel RK, Reddy GB, Dirisala VR.
    Mol Biol Rep; 2020 Oct 01; 47(10):7467-7475. PubMed ID: 32930933
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  • 10. Screening and Functional Analysis of TPO Gene Mutations in a Cohort of Chinese Patients With Congenital Hypothyroidism.
    Wang H, Wang W, Chen X, Shi H, Shi Y, Ding G.
    Front Endocrinol (Lausanne); 2021 Oct 01; 12():774941. PubMed ID: 35002963
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  • 11. Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis.
    Molina MF, Papendieck P, Sobrero G, Balbi VA, Belforte FS, Martínez EB, Adrover E, Olcese MC, Chiesa A, Miras MB, González VG, Pio MG, González-Sarmiento R, Targovnik HM, Rivolta CM.
    Endocrine; 2022 Jun 01; 77(1):86-101. PubMed ID: 35507000
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  • 16. Targeted next-generation sequencing of thirteen causative genes in Chinese patients with congenital hypothyroidism.
    Long W, Lu G, Zhou W, Yang Y, Zhang B, Zhou H, Jiang L, Yu B.
    Endocr J; 2018 Oct 29; 65(10):1019-1028. PubMed ID: 30022773
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