217 related articles for article (PubMed ID: 28849184)
21. [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]
22. Novel EXT1 and EXT2 mutations identified by DHPLC in Italian patients with multiple osteochondromas.
Pedrini E; De Luca A; Valente EM; Maini V; Capponcelli S; Mordenti M; Mingarelli R; Sangiorgi L; Dallapiccola B
Hum Mutat; 2005 Sep; 26(3):280. PubMed ID: 16088908
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. [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]
26. 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]
27. An optimized DHPLC protocol for molecular testing of the EXT1 and EXT2 genes in hereditary multiple osteochondromas.
Wuyts W; Radersma R; Storm K; Vits L
Clin Genet; 2005 Dec; 68(6):542-7. PubMed ID: 16283885
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. [Screening for EXT1 and EXT2 gene mutations in a ethnic Han Chinese family from Shanxi with hereditary multiple exostoses].
Zhou YA; Ma YX; Zhang YH; Hao ZQ; Li XJ; Shi YY; Zhang QB; Li PL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):95-8. PubMed ID: 23450490
[TBL] [Abstract][Full Text] [Related]
31. Mutation analysis and prenatal diagnosis of EXT1 gene mutations in Chinese patients with multiple osteochondromas.
Zhu HY; Hu YL; Yang Y; Wu X; Zhu RF; Zhu XY; Duan HL; Zhang Y; Zhou JY
Chin Med J (Engl); 2011 Oct; 124(19):3054-7. PubMed ID: 22040554
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. New mutations of EXT1 and EXT2 genes in German patients with Multiple Osteochondromas.
Heinritz W; Hüffmeier U; Strenge S; Miterski B; Zweier C; Leinung S; Bohring A; Mitulla B; Peters U; Froster UG
Ann Hum Genet; 2009 May; 73(Pt 3):283-91. PubMed ID: 19344451
[TBL] [Abstract][Full Text] [Related]
34. [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]
35. 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]
36. Determination of the mutation spectrum of the EXT1/EXT2 genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes in EXT negative cases.
Lonie L; Porter DE; Fraser M; Cole T; Wise C; Yates L; Wakeling E; Blair E; Morava E; Monaco AP; Ragoussis J
Hum Mutat; 2006 Nov; 27(11):1160. PubMed ID: 17041877
[TBL] [Abstract][Full Text] [Related]
37. [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]
38. 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]
39. Identification of a novel mutation in EXT2 in a fourth-generation Korean family with multiple osteochondromas and overview of mutation spectrum.
Yang A; Kim J; Jang JH; Lee C; Lee JE; Cho SY; Jin DK
Ann Hum Genet; 2019 May; 83(3):160-170. PubMed ID: 30730578
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
