A polymorphism in intron 2 of the TP53 gene

Clinical Genetics

Volumn 50, Issue 2, 1996, Pages 108-109

  DiCioccio, Richard A ^a   Piver, M Steven ^a  

^a ROSWELL PARK CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CHROMOSOME 17P; CODOMINANCE; DNA POLYMORPHISM; EXON; GENE FREQUENCY; HUMAN; INTRON; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

EID: 0029906997     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1996.tb02360.x     Document Type: Article

References (3)

1. Malkin D. p53 and the Li-Fraumeni syndrome. Biochim Biophys Acta 1994: 1198: 197-213.
2. Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucl Acids Res 1988: 10: 1215.
3. Okamoto A, Sameshima Y, Yokoyama S, Terashima Y, Sugimura T, Terada M, Yokota J. Frequent allelic losses and mutations of the p53 gene in human ovarian cancer. Cancer Res 1991: 51: 5171-5176.