Number of rare germline CNVs and TP53 mutation types.

Orphanet journal of rare diseases

Volumn 7, Issue , 2012, Pages

  Silva, Amanda G ^a   Achatz, Isabel Maria W ^b   Krepischi, Ana Cv ^b   Pearson, Peter L ^b   Rosenberg, Carla ^b  

^a AC Camaargo Hospital   (Brazil)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN P53;

ARTICLE; BRAZIL; COPY NUMBER VARIATION; FAMILIAL CANCER; FEMALE; GENETICS; GENOTYPE; HUMAN; MALE; MUTATION;

BRAZIL; DNA COPY NUMBER VARIATIONS; FEMALE; GENOTYPE; GERM-LINE MUTATION; HUMANS; LI-FRAUMENI SYNDROME; MALE; TUMOR SUPPRESSOR PROTEIN P53;

EID: 84871373385     PISSN: None     EISSN: 17501172     Source Type: None    
DOI: 10.1186/1750-1172-7-101     Document Type: Article

References (0)