Number of rare germline CNVs and TP53 mutation types

Authors: Silva Amanda G, Achatz Isabel Maria W, Krepischi Ana CV, Pearson Peter L, Rosenberg Carla

Source: Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 101 (2012)

Subject Terms: TP53, R337H, Li-Fraumeni syndrome, CNV, Penetrance, Medicine

File Description: electronic resource

Relation: http://www.ojrd.com/content/7/1/101; https://doaj.org/toc/1750-1172

Access URL: https://doaj.org/article/e9d839f1d00f44d6b327149402ea5cc6