Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Abnormalities and NHP2[original query] |
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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 |
Detection of mutations in TERT, the genes for telomerase reverse transcriptase, in Indian patients of aplastic anaemia: a pilot study. The Journal of the Association of Physicians of India 2014 Oct 62 (10): 13-7. Mehta Sudhir, Krishnamohan M, Gulati Sandhya, Sharmat Nidhi, Vashishtha Puneet, Singh Ishw |
[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 |
Dysregulation of H/ACA ribonucleoprotein components in chronic lymphocytic leukemia. PloS one 2017 12 (6): e0179883. Dos Santos Patricia Carolina, Panero Julieta, Stanganelli Carmen, Palau Nagore Virginia, Stella Flavia, Bezares Raimundo, Slavutsky Ir |
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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