BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 33596140)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Identification of a novel EXT2 frameshift mutation in a family with hereditary multiple exostoses by whole-exome sequencing.
    Yang M; Xie H; Xu B; Xiang Q; Wang H; Hu T; Liu S
    J Clin Lab Anal; 2021 Sep; 35(9):e23968. PubMed ID: 34403521
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of mutations in EXT1 and EXT2 in Brazilian patients with multiple osteochondromas.
    Santos SCL; Rizzo IMPO; Takata RI; Speck-Martins CE; Brum JM; Sollaci C
    Mol Genet Genomic Med; 2018 May; 6(3):382-392. PubMed ID: 29529714
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel and recurrent mutations in the EXT1 and EXT2 genes in Chinese kindreds with multiple osteochondromas.
    Wu Y; Xing X; Xu S; Ma H; Cao L; Wang S; Luo Y
    J Orthop Res; 2013 Sep; 31(9):1492-9. PubMed ID: 23629877
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of mutations in EXT1 and EXT2 genes in six Chinese families with multiple osteochondromas.
    Xu Y; Kang Q; Zhang Z
    Mol Med Rep; 2017 Oct; 16(4):5599-5605. PubMed ID: 28849184
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Large-scale mutational analysis in the EXT1 and EXT2 genes for Japanese patients with multiple osteochondromas.
    Ishimaru D; Gotoh M; Takayama S; Kosaki R; Matsumoto Y; Narimatsu H; Sato T; Kimata K; Akiyama H; Shimizu K; Matsumoto K
    BMC Genet; 2016 Mar; 17():52. PubMed ID: 26961984
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation analysis of hereditary multiple exostoses in the Chinese.
    Xu L; Xia J; Jiang H; Zhou J; Li H; Wang D; Pan Q; Long Z; Fan C; Deng HX
    Hum Genet; 1999; 105(1-2):45-50. PubMed ID: 10480354
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel Mutations in Chinese Patients with Multiple Osteochondromas Identified Using Whole Exome Sequencing.
    Tong Y; Luo J; Zhang Y; Hong Z; Cao L; Chen X; Chen J; Bi Q
    Genet Test Mol Biomarkers; 2021 May; 25(5):361-367. PubMed ID: 34003695
    [No Abstract]   [Full Text] [Related]  

  • 12. A Novel Nonsense Mutation in the
    Chen Z; Ruan W; Li M; Cao L; Lu J; Zhong F; Bi Q
    Genet Test Mol Biomarkers; 2020 Aug; 24(8):478-483. PubMed ID: 32678989
    [No Abstract]   [Full Text] [Related]  

  • 13. A Novel Intronic Splicing Mutation in the
    Guo X; Chen S; Lin M; Pan Y; Liu N; Shi T
    Genet Test Mol Biomarkers; 2021 Jul; 25(7):478-485. PubMed ID: 34280007
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. A Novel EXT1 Mutation Identified in a Family with Multiple Osteochondromas.
    Chen Z; Bi Q; Kong M; Chen Y
    Genet Test Mol Biomarkers; 2019 Apr; 23(4):251-254. PubMed ID: 29989442
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in the EXT1 and EXT2 genes in hereditary multiple exostoses.
    Wuyts W; Van Hul W; De Boulle K; Hendrickx J; Bakker E; Vanhoenacker F; Mollica F; Lüdecke HJ; Sayli BS; Pazzaglia UE; Mortier G; Hamel B; Conrad EU; Matsushita M; Raskind WH; Willems PJ
    Am J Hum Genet; 1998 Feb; 62(2):346-54. PubMed ID: 9463333
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Mutation screening of the EXT1 and EXT2 genes in patients with hereditary multiple exostoses.
    Philippe C; Porter DE; Emerton ME; Wells DE; Simpson AH; Monaco AP
    Am J Hum Genet; 1997 Sep; 61(3):520-8. PubMed ID: 9326317
    [TBL] [Abstract][Full Text] [Related]  

  • 19. One third of Japanese patients with multiple osteochondromas may have mutations in genes other than EXT1 or EXT2.
    Kojima H; Wada T; Seki H; Kubota T; Wakui K; Fukushima Y
    Genet Test; 2008 Dec; 12(4):557-61. PubMed ID: 18976157
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [A new EXT2 mutation in a Chinese family with hereditary multiple exostoses].
    Zhao WQ; Song SJ; Wei Q; Qiao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):241-4. PubMed ID: 19504431
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.