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Journal of Korean Medical Science|April 7, 2026
Perception of Family Genetic Testing for Hereditary Breast and Ovarian Cancer: A Survey of Patients and General PublicEun Jeong Lee, Ji Young Kim, Jiwoo An, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 23, 2009
New lesions detected by single nucleotide polymorphism array-based chromosomal analysis have important clinical impact in acute myeloid leukemiaRamon V Tiu, Lukasz P Gondek, Christine L O'Keefe, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 11, 2009
Mutations of e3 ubiquitin ligase cbl family members constitute a novel common pathogenic lesion in myeloid malignanciesHideki Makishima, Heather Cazzolli, Hadrian Szpurka, et al.
Blood|February 3, 2011
Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignanciesRamon V Tiu, Lukasz P Gondek, Christine L O'Keefe, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 16, 2011
Adverse prognostic impact of abnormal lesions detected by genome-wide single nucleotide polymorphism array-based karyotyping analysis in acute myeloid leukemia with normal karyotypeJun Ho Yi, Jungwon Huh, Hee-Jin Kim, et al.
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