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Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria.

Muir-Torre syndrome (MTS) is an autosomal dominant disease defined by the coincidence of at least one sebaceous skin tumor and one internal malignancy. About half of MTS patients are affected by colorectal cancer. In a subgroup of MTS patients the disease has an underlying DNA mismatch-repair (MMR)...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Kruse, R, Rütten, A, Lamberti, C, Hosseiny-Malayeri, H R, Wang, Y, Ruelfs, C, Jungck, M, Mathiak, M, Ruzicka, T, Hartschuh, W, Bisceglia, M, Friedl, W, Propping, P
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: 1998
Θέματα:
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377247/
https://ncbi.nlm.nih.gov/pubmed/9634524
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