Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors.

The Beckwith-Wiedemann syndrome (BWS) is marked by fetal organ overgrowth and conveys a predisposition to certain childhood tumors, including Wilms tumor (WT). The genetics of BWS have implicated a gene that maps to chromosome 11p15 and is paternally imprinted, and the gene encoding the cyclin-cdk i...

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שמור ב:
מידע ביבליוגרפי
Main Authors: O'Keefe, D, Dao, D, Zhao, L, Sanderson, R, Warburton, D, Weiss, L, Anyane-Yeboa, K, Tycko, B
פורמט: Artigo
שפה:Inglês
יצא לאור: 1997
נושאים:
Research Article
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715902/
https://ncbi.nlm.nih.gov/pubmed/9311733
תגים: הוספת תג
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