Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Abnormalities and TERC[original query] |
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Mutations in the SBDS gene in acquired aplastic anemia. Blood 2007 Aug 110 (4): 1141-6. Calado Rodrigo T, Graf Solomon A, Wilkerson Keisha L, Kajigaya Sachiko, Ancliff Philip J, Dror Yigal, Chanock Stephen J, Lansdorp Peter M, Young Neal |
TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes. Blood 2008 Nov 112 (9): 3594-600. Walne Amanda J, Vulliamy Tom, Beswick Richard, Kirwan Michael, Dokal Inderje |
Telomerase gene mutation screening and telomere overhang detection in Chinese patients with acute myeloid leukemia. Leukemia & lymphoma 2013 Jul 54 (7): 1437-41. Yan Siyi, Han Bing, Wu Yongji, Zhou Daobin, Zhao Yongqia |
[Genotype analysis and telomere length measure in patients with dyskeratosis congenita]. Zhongguo shi yan xue ye xue za zhi / Zhongguo bing li sheng li xue hui = Journal of experimental hematology / Chinese Association of Pathophysiology 2015 Feb 23 (1): 212-6. Zhang Jia-Yuan, An Wen-Bin, Zhang Li, Chang Li-Xian, Qi Ben-Quan, Liu Tian-Feng, Liu Fang, Yang Wen-Yu, Guo Ye, Zhu Xiao-F |
Integrating Genomics Into Management of Fibrotic Interstitial Lung Disease. Chest 2019 1 155 (5): 1026-1040. Adegunsoye Ayodeji, Vij Rekha, Noth Im |
Pulmonary fibrosis in dyskeratosis congenita: a case report with a PRISMA-compliant systematic review. BMC pulmonary medicine 2021 9 21 (1): 279. Wang Ping, Xu Zuoj |
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- Page last updated:Apr 16, 2024
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