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 *

124 related articles for article (PubMed ID: 10738008)

  • 1. An R223P mutation in EXT2 gene causes hereditary multiple exostoses.
    Shi YR; Wu JY; Tsai FJ; Lee CC; Tsai CH
    Hum Mutat; 2000 Apr; 15(4):390-1. PubMed ID: 10738008
    [No Abstract]   [Full Text] [Related]  

  • 2. Gene for multiple exostoses (EXT2) maps to 11(p11.2p12) and is deleted in patients with a contiguous gene syndrome.
    Ligon AH; Potocki L; Shaffer LG; Stickens D; Evans GA
    Am J Med Genet; 1998 Feb; 75(5):538-40. PubMed ID: 9489802
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. [From gene to disease; hereditary multiple exostoses].
    Wuyts W; Bovée JV; Hogendoorn PC
    Ned Tijdschr Geneeskd; 2002 Jan; 146(4):162-4. PubMed ID: 11845565
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 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. A novel splice site mutation of the EXT2 gene in a Finnish hereditary multiple exostoses family. Mutations in brief no. 197. Online.
    Wolf M; Hemminki A; Kivioja A; Sistonen P; Kaitila I; Ervasti H; Kinnunen J; Karaharju E; Knuutila S
    Hum Mutat; 1998; 12(5):362. PubMed ID: 10671060
    [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 new polymorphism (c28C>A) of EXT2 gene identified in a Taiwan Chinese family.
    Shi YR; Wu JY; Tsai FJ; Lee CC; Tsai CH
    Hum Mutat; 2001 Apr; 17(4):356. PubMed ID: 11295850
    [No Abstract]   [Full Text] [Related]  

  • 13. The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes.
    Stickens D; Clines G; Burbee D; Ramos P; Thomas S; Hogue D; Hecht JT; Lovett M; Evans GA
    Nat Genet; 1996 Sep; 14(1):25-32. PubMed ID: 8782816
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. Molecular basis of multiple exostoses: mutations in the EXT1 and EXT2 genes.
    Wuyts W; Van Hul W
    Hum Mutat; 2000; 15(3):220-7. PubMed ID: 10679937
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Assessing the general population frequency of rare coding variants in the EXT1 and EXT2 genes previously implicated in hereditary multiple exostoses.
    Cousminer DL; Arkader A; Voight BF; Pacifici M; Grant SFA
    Bone; 2016 Nov; 92():196-200. PubMed ID: 27616605
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The EXT2 gene mutation in a family with hereditary multiple exostoses].
    Yao F; Wang Y; Liao S; Wang L; Wang T; Kang B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Feb; 27(1):92-5. PubMed ID: 20140877
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan.
    Shi YR; Wu JY; Hsu YA; Lee CC; Tsai CH; Tsai FJ
    Genet Test; 2002; 6(3):237-43. PubMed ID: 12490068
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.