Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Abnormalities and EPO[original query] |
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Clinical relevance of hemochromatosis-related HFE C282Y/H63D gene mutations in patients on chronic dialysis. Clinical nephrology 2002 Dec 58 (6): 438-44. Canavese C, Bergamo D, Barbieri S, Timbaldi M, Thea A, Martina G, Damiani D, Fenoglio R, Donati-Marella B, Priolo |
Cytogenetic abnormalities and genomic copy number variations in EPO (7q22) and SEC-61(7p11) genes in primary myelodysplastic syndromes. Blood cells, molecules & diseases 2016 Jul 59 52-7. Mohanty Purvi, Korgaonkar Seema, Shanmukhaiah Chandrakala, Ghosh Kanjaksha, Vundinti Babu R |
Erythropoietin Concentration in Boys With p.His63Asp Polymorphism of the HFE Gene. Journal of pediatric hematology/oncology 2021 2 44 (1): e68-e73. Kaczorowska-Hac Barbara, Luszczyk Marcin, Wasilewska Eliza, Antosiewicz Jedrzej, Kaczor Jan |
Prediction of Response to Erythropoiesis Stimulating Agents in Low-Risk Myelodysplastic Syndromes. Asian Pacific journal of cancer prevention : APJCP 2021 12 22 (12): 4037-4042. Hattakitpanitchakul Saroj, Kobbuaklee Sirorat, Wudhikarn Kitsada, Polprasert Chanta |
Two Novel Genetic Variants Involved in the Oxygen Sensing Pathway in JAK2-unmutated Erythrocytosis. Biochemical genetics 2024 4 . Qiang Ma, Ronghua Hu, Wuhan Hui, Hong Zhao, Dongmei Zou, Yan Liu, Wanling S |
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- Page last updated:Apr 22, 2024
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