Common pattern of unusual chromosome abnormalities in hereditary papillary renal carcinoma

Cancer Genetics and Cytogenetics

Volumn 164, Issue 2, 2006, Pages 142-147

  Prat, Esther ^a   Bernués, Marta ^b   Del Rey, Javier ^a   Camps, Jordi ^a   Ponsa, Immaculada ^a   Algaba, Ferran ^a   Egozcue, Josep ^a   Caballín, Ma Rosa ^a   Gelabert, Antoni ^c   Miró, Rosa ^a  

^a UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^b HOSPITAL UNIVERSITARIO SON ESPASES   (Spain)

^c HOSPITAL DEL MAR   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN TYROSINE KINASE; SCATTER FACTOR RECEPTOR;

ARTICLE; CASE REPORT; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME TRANSLOCATION 15; CHROMOSOME TRANSLOCATION 2; COMPARATIVE GENOMIC HYBRIDIZATION; FAMILIAL CANCER; GENE FREQUENCY; GENE MUTATION; GENETIC SUSCEPTIBILITY; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; KIDNEY CARCINOMA; MALE; NUCLEOTIDE SEQUENCE; PAPILLARY CARCINOMA; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTO ONCOGENE; TRISOMY; TRISOMY 12; TRISOMY 13; TRISOMY 17; TRISOMY 7;

CARCINOMA, PAPILLARY; CARCINOMA, RENAL CELL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 7; HUMANS; KIDNEY NEOPLASMS; MALE; MUTATION; NUCLEIC ACID HYBRIDIZATION; PEDIGREE; PROTO-ONCOGENE PROTEINS C-MET;

EID: 31144478674     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2005.09.010     Document Type: Article

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