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 *

290 related articles for article (PubMed ID: 18810975)

  • 1. Novel mutation in the EXT-1 gene in an Iranian family affected with hereditary multiple exostoses.
    Foroughmand AM; Galehdari H; Rasouli M; Mohammadian G; Mohammadi M
    Pak J Biol Sci; 2008 Apr; 11(7):1037-41. PubMed ID: 18810975
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. [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]  

  • 8. Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis).
    Faiyaz-Ul-Haque M; Ahmad W; Zaidi SH; Hussain S; Haque S; Ahmad M; Cohn DH; Tsui LC
    Clin Genet; 2004 Aug; 66(2):144-51. PubMed ID: 15253765
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genotype-phenotype correlation in hereditary multiple exostoses.
    Francannet C; Cohen-Tanugi A; Le Merrer M; Munnich A; Bonaventure J; Legeai-Mallet L
    J Med Genet; 2001 Jul; 38(7):430-4. PubMed ID: 11432960
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. 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]  

  • 12. [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]  

  • 13. 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]  

  • 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. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Evaluation of locus heterogeneity and EXT1 mutations in 34 families with hereditary multiple exostoses.
    Raskind WH; Conrad EU; Matsushita M; Wijsman EM; Wells DE; Chapman N; Sandell LJ; Wagner M; Houck J
    Hum Mutat; 1998; 11(3):231-9. PubMed ID: 9521425
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 15.