Late-onset common cancers in a kindred with an Arg213Gln TP53 germline mutation

Familial Cancer

Volumn 5, Issue 2, 2006, Pages 169-174

  Ruijs, Mariëlle W G ^a,b   Verhoef, Senno ^a   Wigbout, Gea ^a   Pruntel, Roelof ^a   Floore, Arno N ^a   De Jong, Daphne ^a   Van 'T Veer, Laura J ^a   Menko, Fred H ^b  

^a NETHERLANDS CANCER INSTITUTE   (Netherlands)

^b VU UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

FASAY; Li Fraumeni syndrome; Li Fraumeni like syndrome; Missense mutation; TP53

Indexed keywords

ARGININE; GLYCINE; PROTEIN P53;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BREAST CANCER; CANCER SUSCEPTIBILITY; CLINICAL ARTICLE; COLORECTAL CANCER; FAMILIAL CANCER; FEMALE; GENE MUTATION; GENETIC TRANSCRIPTION; HUMAN; IN VITRO STUDY; KIDNEY CARCINOMA; MALE; MELANOMA; ONSET AGE; OVARY CANCER; PATIENT SELECTION; PEDIGREE; PRIORITY JOURNAL; SARCOMA; STOMACH CANCER;

ADULT; AGED; FEMALE; GENES, P53; GERM-LINE MUTATION; HETEROZYGOTE; HUMANS; LI-FRAUMENI SYNDROME; MIDDLE AGED; NEOPLASMS;

EID: 33744760870     PISSN: 13899600     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10689-005-4789-9     Document Type: Article

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