Sporadic breast cancers exhibit loss of heterozygosity on chromosome segment 10q23 close to the Cowden disease locus

Genes Chromosomes and Cancer

Volumn 21, Issue 2, 1998, Pages 166-171

  Singh, Baljit ^a   Ittmann, Michael M ^b,c   Krolewski, John J ^a  

^a The New York Presbyterian Hospital   (United States)

^b VETERANS AFFAIRS MEDICAL CENTER   (United States)

^c MICHAEL E DEBAKEY VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADULT; AGED; ALLELE; ARTICLE; AUTORADIOGRAPHY; BREAST CANCER; CANCER SUSCEPTIBILITY; CHROMOSOME 10Q; CHROMOSOME DELETION; CLINICAL ARTICLE; CONTROLLED STUDY; COWDEN SYNDROME; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PROGNOSIS; TUMOR SUPPRESSOR GENE;

ADENOCARCINOMA, MUCINOUS; ADULT; AGED; AGED, 80 AND OVER; BREAST NEOPLASMS; CARCINOMA, DUCTAL, BREAST; CHROMOSOMES, HUMAN, PAIR 10; HAMARTOMA SYNDROME, MULTIPLE; HUMANS; LOSS OF HETEROZYGOSITY; MIDDLE AGED;

EID: 0031916211     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199802)21:2<166::AID-GCC13>3.0.CO;2-P     Document Type: Article

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