p53 germline mutation in a patient with Li-Fraumeni Syndrome and three metachronous malignancies

Journal of Cancer Research and Clinical Oncology

Volumn 128, Issue 8, 2002, Pages 456-460

  Pötzsch, Claudia ^a   Voigtländer, Theda ^b   Lübbert, Michael ^a  

^a UNIVERSITY OF FREIBURG   (Germany)

^b UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

Hereditary cancer; Melanoma; Second primary neoplasm; Tumor suppressor gene

Indexed keywords

ARGININE; HISTIDINE;

ADRENAL CORTEX CARCINOMA; AMINO ACID SUBSTITUTION; ARTICLE; BRAIN TUMOR; BREAST CANCER; CASE REPORT; CODON; CONTROLLED STUDY; DIAGNOSTIC TEST; DNA EXTRACTION; DNA SEQUENCE; EPITHELIUM TUMOR; EXON; FAMILIAL CANCER; FEMALE; GENE MUTATION; GENETIC COUNSELING; GENETIC DISORDER; GERM LINE; HUMAN; HUMAN CELL; INFORMED CONSENT; LARYNX CANCER; LEIOMYOSARCOMA; LEUKEMIA; MELANOMA; MONONUCLEAR CELL; PRIORITY JOURNAL; PROSTATE CANCER; SARCOMA; STOMACH CANCER;

ADULT; CODON; EXONS; FAMILY HEALTH; FEMALE; GENES, P53; GERM-LINE MUTATION; HUMANS; LI-FRAUMENI SYNDROME; MALE; NEOPLASMS, MULTIPLE PRIMARY; PEDIGREE;

EID: 0036037491     PISSN: 01715216     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00432-002-0360-3     Document Type: Article

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