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المؤلفون: Helderman, N.C., Elsayed, F.A., Wezel, T. van, Terlouw, D., Langers, A.M.J., Egmond, D. van, Kilinc, G., Hristova, H., Sarasqueta, A.F., Morreau, H., Nielsen, M., Suerink, M.
المساهمون: Pathology
المصدر: Human pathology, 125, 11-17. W.B. Saunders Ltd
Human Pathology, 125, 11-17. W B SAUNDERS CO-ELSEVIER INCمصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, MUTYH, Brain Neoplasms, Colorectal Neoplasms, Hereditary Nonpolyposis, DNA Mismatch Repair, Pathology and Forensic Medicine, DNA Glycosylases, Neuroendocrine Tumors, Lynch syndrome, Neoplastic Syndromes, Hereditary, Intestine, Small, Humans, Small intestine-neuroendocrine tumors, Colorectal Neoplasms, MutL Protein Homolog 1, Cancer genetics, Mismatch repair deficiency, Germ-Line Mutation, Mismatch Repair Endonuclease PMS2
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