217 related articles for article (PubMed ID: 28849184)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Mutation screening of EXT genes in Chinese patients with multiple osteochondromas.
Kang Z; Peng F; Ling T
Gene; 2012 Sep; 506(2):298-300. PubMed ID: 22820392
[TBL] [Abstract][Full Text] [Related]
8. Novel mutation of EXT2 identified in a large family with multiple osteochondromas.
Chen XJ; Zhang H; Tan ZP; Hu W; Yang YF
Mol Med Rep; 2016 Nov; 14(5):4687-4691. PubMed ID: 27748933
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. Targeted Next-Generation Sequencing Newly Identifies Mutations in Exostosin-1 and Exostosin-2 Genes of Patients with Multiple Osteochondromas.
Guo X; Lin M; Shi T; Yan W; Chen W
Tohoku J Exp Med; 2017 Jul; 242(3):173-181. PubMed ID: 28690282
[TBL] [Abstract][Full Text] [Related]
13. Ext-mutation analysis in Italian sporadic and hereditary osteochondromas.
Gigante M; Matera MG; Seripa D; Izzo AM; Venanzi R; Giannotti A; Digilio MC; Gravina C; Lazzari M; Monteleone G; Monteleone M; Dallapiccola B; Fazio VM
Int J Cancer; 2001 Nov; 95(6):378-83. PubMed ID: 11668521
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Ulna/height ratio as clinical parameter separating EXT1 from EXT2 families?
Leube B; Hardt K; Portier S; Westhoff B; Jäger M; Krauspe R; Royer-Pokora B
Genet Test; 2008 Mar; 12(1):129-33. PubMed ID: 18373409
[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. [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]
18. 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]
19. 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]
20. Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromas.
Sarrión P; Sangorrin A; Urreizti R; Delgado A; Artuch R; Martorell L; Armstrong J; Anton J; Torner F; Vilaseca MA; Nevado J; Lapunzina P; Asteggiano CG; Balcells S; Grinberg D
Sci Rep; 2013; 3():1346. PubMed ID: 23439489
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]