Silva, Amanda G

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