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 *

204 related articles for article (PubMed ID: 31030431)

  • 1. [Analysis of EXT1 and EXT2 gene mutations in two Chinese pedigrees affected with hereditary multiple exostosis].
    Bai Y; Liu N; Hu S; Wu Q; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 May; 36(5):451-455. PubMed ID: 31030431
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Genetic analysis of five pedigrees affected with multiple osteochondromas].
    Bai Y; Jiao Z; Liu N; Hu S; Zhao K; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul; 37(7):717-720. PubMed ID: 32619249
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Identification of a novel EXT1 mutation in a pedigree affected with hereditary multiple exostosis].
    Lou G; Yang K; Qin L; Zhang Y; Wang H; Hou Q; He M; Liao S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):91-95. PubMed ID: 29419870
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel EXT1 and EXT2 mutations in hereditary multiple exostoses families of Indian origin.
    Vanita V; Sperling K; Sandhu HS; Sandhu PS; Singh JR
    Genet Test Mol Biomarkers; 2009 Feb; 13(1):43-9. PubMed ID: 19309273
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostoses.
    Al-Zayed Z; Al-Rijjal RA; Al-Ghofaili L; BinEssa HA; Pant R; Alrabiah A; Al-Hussainan T; Zou M; Meyer BF; Shi Y
    Orphanet J Rare Dis; 2021 Feb; 16(1):100. PubMed ID: 33632255
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 20 novel point mutations and one large deletion in EXT1 and EXT2 genes: report of diagnostic screening in a large Italian cohort of patients affected by hereditary multiple exostosis.
    Ciavarella M; Coco M; Baorda F; Stanziale P; Chetta M; Bisceglia L; Palumbo P; Bengala M; Raiteri P; Silengo M; Caldarini C; Facchini R; Lala R; Cavaliere ML; De Brasi D; Pasini B; Zelante L; Guarnieri V; D'Agruma L
    Gene; 2013 Feb; 515(2):339-48. PubMed ID: 23262345
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Identification of pathogenic variations in two Chinese pedigrees affected with hereditary multiple exostosis].
    You Y; Li S; Yang B; Zhao X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Aug; 36(8):757-760. PubMed ID: 31400121
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of Novel EXT Mutations in Patients with Hereditary Multiple Exostoses Using Whole-Exome Sequencing.
    Liang C; Wang YJ; Wei YX; Dong Y; Zhang ZC
    Orthop Surg; 2020 Jun; 12(3):990-996. PubMed ID: 32293802
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutational screening of EXT1 and EXT2 genes in Polish patients with hereditary multiple exostoses.
    Jamsheer A; Socha M; Sowińska-Seidler A; Telega K; Trzeciak T; Latos-Bieleńska A
    J Appl Genet; 2014 May; 55(2):183-8. PubMed ID: 24532482
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Mutation analysis of EXT2 gene in a family with hereditary multiple exostosis].
    Li L; Li X; Liu Y; Zheng S; Zhang J; Liu Q; Heng X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):743-6. PubMed ID: 25449079
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of pathogenic mutations in 6 Chinese families with multiple exostoses by whole-exome sequencing and multiplex ligation-dependent probe amplification: Case series.
    Long X; Li Z; Huang Y; Zhang L; Lv W; Teng Y; Linpeng S; Liang D; Wu L
    Medicine (Baltimore); 2019 May; 98(20):e15692. PubMed ID: 31096510
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Mutation analysis of EXT genes in two pedigrees with hereditary multiple exostoses].
    Deng LB; Quan Y; Liu J; Lin Peng SY; Liang DS; Wu LQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Dec; 30(6):641-4. PubMed ID: 24327137
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A splicing mutation of EXT1 in a Chinese pedigree with hereditary multiple exostoses].
    Wang W; Qiu ZQ; Song HM
    Zhongguo Dang Dai Er Ke Za Zhi; 2014 Feb; 16(2):174-80. PubMed ID: 24568913
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Three novel EXT1 and EXT2 gene mutations in Taiwanese patients with multiple exostoses.
    Chen WC; Chi CH; Chuang CC; Jou IM
    J Formos Med Assoc; 2006 May; 105(5):434-7. PubMed ID: 16638657
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Heterogeneous spectrum of EXT gene mutations in Chinese patients with hereditary multiple osteochondromas.
    Li Y; Wang J; Tang J; Wang Z; Han B; Li N; Yu T; Chen Y; Fu Q
    Medicine (Baltimore); 2018 Oct; 97(42):e12855. PubMed ID: 30334991
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A splice mutation and mRNA decay of EXT2 provoke hereditary multiple exostoses.
    Tian C; Yan R; Wen S; Li X; Li T; Cai Z; Li X; Du H; Chen H
    PLoS One; 2014; 9(4):e94848. PubMed ID: 24728384
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutation screening for the EXT1 and EXT2 genes in Chinese patients with multiple osteochondromas.
    Kang QL; Xu J; Zhang Z; He JW; Fu WZ; Zhang ZL
    Arch Med Res; 2013 Oct; 44(7):542-8. PubMed ID: 24120389
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of four novel EXT1 and EXT2 mutations in five Chinese pedigrees with hereditary multiple exostoses.
    Li Y; Wang D; Wang W; Wang J; Li H; Wang J; Wang X; Fu Q
    Genet Test Mol Biomarkers; 2009 Dec; 13(6):825-30. PubMed ID: 19839753
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of Novel Mutations in the
    Tong Y; Zhang Y; Luo J; Hong Z; Chen X; Bi Q
    Genet Test Mol Biomarkers; 2021 Feb; 25(2):145-151. PubMed ID: 33596140
    [No Abstract]   [Full Text] [Related]  

  • 20. Germline mutations in the EXT1 and EXT2 genes in Korean patients with hereditary multiple exostoses.
    Park KJ; Shin KH; Ku JL; Cho TJ; Lee SH; Choi IH; Phillipe C; Monaco AP; Porter DE; Park JG
    J Hum Genet; 1999; 44(4):230-4. PubMed ID: 10429361
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.