Number of rare germline CNVs and TP53 mutation types. [electronic resource]
- Orphanet journal of rare diseases Dec 2012
- 101 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1750-1172
10.1186/1750-1172-7-101 doi
Brazil DNA Copy Number Variations--genetics Female Genotype Germ-Line Mutation--genetics Humans Li-Fraumeni Syndrome--genetics Male Tumor Suppressor Protein p53--genetics