Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Monosomy and SRSF2[original query] |
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| Clinical implications of the SETBP1 mutation in patients with primary myelodysplastic syndrome and its stability during disease progression. American journal of hematology 2014 Feb 89 (2): 181-6. Hou Hsin-An, Kuo Yuan-Yeh, Tang Jih-Luh, Chou Wen-Chien, Yao Ming, Lai Yan-Jun, Lin Chien-Chin, Chen Chien-Yuan, Liu Chieh-Yu, Tseng Mei-Hsuan, Huang Chi-Fei, Chiang Ying-Chieh, Lee Fen-Yu, Liu Ming-Chih, Liu Chia-Wen, Huang Shang-Yi, Ko Bor-Sheng, Wu Shang-Ju, Tsay Woei, Chen Yao-Chang, Tien Hwei-Fa |
| Incidence and prognostic impact of cytogenetic aberrations in patients with systemic mastocytosis. Genes, chromosomes & cancer 2018 Jan . Naumann Nicole, Jawhar Mohamad, Schwaab Juliana, Kluger Sebastian, Lübke Johannes, Metzgeroth Georgia, Popp Henning D, Khaled Nada, Horny Hans-Peter, Sotlar Karl, Valent Peter, Haferlach Claudia, Göhring Gudrun, Schlegelberger Brigitte, Meggendorfer Manja, Hofmann Wolf-Karsten, Cross Nicholas C P, Reiter Andreas, Fabarius Ali |
| The Genetics of Uveal Melanoma: Overview and Clinical Relevance. Klinische Monatsblatter fur Augenheilkunde 2021 8 238 (7): 773-780. Riechardt Aline Isabel, Kilic Emine, Joussen Antonia |
| A novel heptasomy 21 associated with complete loss of heterozygosity and loss of function RUNX1 mutation in acute myeloid leukemia. Cancer genetics 2022 7 266-267 69-73. Yang Fei, Akkari Yassmine, Fan Guang, Olson Susan, Moore Steph |
| Sex Disparities in Myelodysplastic Syndromes: Genotype, Phenotype, and Outcomes. Clinical lymphoma, myeloma & leukemia 2023 2 . Tinsley-Vance Sara M, Ali Najla Al, Ball Somedeb, Aguirre Luis E, Jain Akriti G, Hussaini Mohammad Omar, Chan Onyee, Kuykendall Andrew, Sweet Kendra, Lancet Jeffrey, Padron Eric, Sallman David A, Komrokji Rami |
- Page last reviewed:Feb 1, 2023
- Page last updated:May 22, 2023
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