144 related articles for article (PubMed ID: 25907943)
1. [Clinical features and genotype analysis in a case of dyskeratosis congenita].
Yuan SS; Lu YD; Wu CL; Li HP; Ge H; Zhang YM
Nan Fang Yi Ke Da Xue Xue Bao; 2015 Apr; 35(4):553-6. PubMed ID: 25907943
[TBL] [Abstract][Full Text] [Related]
2. [Dyskeratosis congenital: clinical features and genotype analysis in two Chinese patients].
Liu R; Shi XD; Wang TY; Liu ZQ; Hu T; Fan W; Cao J; Hou R; Liang C; Huang SA
Zhonghua Xue Ye Xue Za Zhi; 2011 Oct; 32(10):684-7. PubMed ID: 22339828
[TBL] [Abstract][Full Text] [Related]
3. [Genotype analysis and telomere length measure in patients with dyskeratosis congenita].
Zhang JY; An WB; Zhang L; Chang LX; Qi BQ; Liu TF; Liu F; Yang WY; Guo Y; Zhu XF
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2015 Feb; 23(1):212-6. PubMed ID: 25687075
[TBL] [Abstract][Full Text] [Related]
4. [Clinical and genetic features of dyskeratosis congenital with bone marrow failure in eight patients].
Wan Y; An WB; Zhang JY; Zhang JL; Zhang RR; Zhu S; Chang LX; Zhang YC; Liu F; Yang WY; Chen XJ; Zou Y; Chen YM; Zhu XF
Zhonghua Xue Ye Xue Za Zhi; 2016 Mar; 37(3):216-20. PubMed ID: 27033759
[TBL] [Abstract][Full Text] [Related]
5. High resolution melting analysis for the identification of novel mutations in DKC1 and TERT genes in patients with dyskeratosis congenita.
Carrillo J; Martínez P; Solera J; Moratilla C; González A; Manguán-García C; Aymerich M; Canal L; Del Campo M; Dapena JL; Escoda L; García-Sagredo JM; Martín-Sala S; Rives S; Sevilla J; Sastre L; Perona R
Blood Cells Mol Dis; 2012 Oct 15-Dec 15; 49(3-4):140-6. PubMed ID: 22664374
[TBL] [Abstract][Full Text] [Related]
6. Pulmonary fibrosis in dyskeratosis congenita: a case report with a PRISMA-compliant systematic review.
Wang P; Xu Z
BMC Pulm Med; 2021 Sep; 21(1):279. PubMed ID: 34479523
[TBL] [Abstract][Full Text] [Related]
7. Dyskeratosis congenita with a novel genetic variant in the DKC1 gene: a case report.
Ratnasamy V; Navaneethakrishnan S; Sirisena ND; Grüning NM; Brandau O; Thirunavukarasu K; Dagnall CL; McReynolds LJ; Savage SA; Dissanayake VHW
BMC Med Genet; 2018 May; 19(1):85. PubMed ID: 29801475
[TBL] [Abstract][Full Text] [Related]
8. Long-Term Follow-Up of a Case with Dyskeratosis Congenita Caused by NHP2-V126M/X154R Mutation: Genotype-Phenotype Association.
Erdem M; Tüfekçi Ö; Yılmaz Ş; Alacacıoğlu İ; Ören H
Acta Haematol; 2019; 141(1):28-31. PubMed ID: 30472699
[TBL] [Abstract][Full Text] [Related]
9. [Clinical and genetic characteristics of a patient with dyskeratosis congenita].
Li JG; Li Y; Lin ZM; Ma ZH; Li JH; Liu R; Shi XD; Yang Y; Wang TY
Zhonghua Er Ke Za Zhi; 2009 Nov; 47(11):867-70. PubMed ID: 20079002
[TBL] [Abstract][Full Text] [Related]
10. Clinical features of dyskeratosis congenita in mainland China: case reports and literature review.
Li F; Li W; Qiao X; Xie X
Int J Hematol; 2019 Mar; 109(3):328-335. PubMed ID: 30604317
[TBL] [Abstract][Full Text] [Related]
11. Advances in the understanding of dyskeratosis congenita.
Walne AJ; Dokal I
Br J Haematol; 2009 Apr; 145(2):164-72. PubMed ID: 19208095
[TBL] [Abstract][Full Text] [Related]
12. Sequence analysis of the shelterin telomere protection complex genes in dyskeratosis congenita.
Savage SA; Giri N; Jessop L; Pike K; Plona T; Burdett L; Alter BP
J Med Genet; 2011 Apr; 48(4):285-8. PubMed ID: 21209122
[TBL] [Abstract][Full Text] [Related]
13. Identification of a novel mutation and a de novo mutation in DKC1 in two Chinese pedigrees with Dyskeratosis congenita.
Ding YG; Zhu TS; Jiang W; Yang Y; Bu DF; Tu P; Zhu XJ; Wang BX
J Invest Dermatol; 2004 Sep; 123(3):470-3. PubMed ID: 15304085
[TBL] [Abstract][Full Text] [Related]
14. TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenita.
Savage SA; Giri N; Baerlocher GM; Orr N; Lansdorp PM; Alter BP
Am J Hum Genet; 2008 Feb; 82(2):501-9. PubMed ID: 18252230
[TBL] [Abstract][Full Text] [Related]
15. Identification of DKC1 gene mutations in Japanese patients with X-linked dyskeratosis congenita.
Kanegane H; Kasahara Y; Okamura J; Hongo T; Tanaka R; Nomura K; Kojima S; Miyawaki T
Br J Haematol; 2005 May; 129(3):432-4. PubMed ID: 15842668
[TBL] [Abstract][Full Text] [Related]
16. Hoyeraal-Hreidarsson syndrome with a DKC1 mutation identified by whole-exome sequencing.
Lim BC; Yoo SK; Lee S; Shin JY; Hwang H; Chae JH; Hwang YS; Seo JS; Kim JI; Kim KJ
Gene; 2014 Aug; 546(2):425-9. PubMed ID: 24914498
[TBL] [Abstract][Full Text] [Related]
17. Dyskeratosis congenita associated with leukoplakia of the tongue.
Noto Z; Tomihara K; Furukawa K; Noguchi M
Int J Oral Maxillofac Surg; 2016 Jun; 45(6):760-3. PubMed ID: 26778687
[TBL] [Abstract][Full Text] [Related]
18. Identification of a novel mutation in DKC1 in dyskeratosis congenita.
Kurnikova M; Shagina I; Khachatryan L; Schagina O; Maschan M; Shagin D
Pediatr Blood Cancer; 2009 Jan; 52(1):135-7. PubMed ID: 18802941
[TBL] [Abstract][Full Text] [Related]
19. A novel missense mutation in the DKC1 gene in a Japanese family with X-linked dyskeratosis congenita.
Hiramatsu H; Fujii T; Kitoh T; Sawada M; Osaka M; Koami K; Irino T; Miyajima T; Ito M; Sugiyama T; Okuno T
Pediatr Hematol Oncol; 2002 Sep; 19(6):413-9. PubMed ID: 12186364
[TBL] [Abstract][Full Text] [Related]
20. Dyskeratosis congenita--two siblings with a new missense mutation in the DKC1 gene.
Coelho JD; Lestre S; Kay T; Lopes MJ; Fiadeiro T; Apetato M
Pediatr Dermatol; 2011; 28(4):464-6. PubMed ID: 21736606
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
