Childhood predictive genetic testing for Li-Fraumeni syndrome

Familial Cancer

Volumn 9, Issue 1, 2010, Pages 65-69

  Evans, D G ^a   Lunt, P ^b   Clancy, T ^a   Eeles, R ^c  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

^b ST MICHAEL'S HOSPITAL   (United Kingdom)

^c INSTITUTE OF CANCER RESEARCH   (United Kingdom)

Author keywords

Childhood; Genetic testing; Li Fraumeni; Presymptomatic; TP53

Indexed keywords

BRCA1 PROTEIN; PROTEIN P53;

ARTICLE; ASTROCYTOMA; BRAIN TUMOR; BREAST CANCER; CANCER RISK; CASE REPORT; CHILD; FAMILIAL CANCER; FEMALE; GENE MUTATION; GENETIC COUNSELING; GENETIC SCREENING; HUMAN; LEIOMYOSARCOMA; MALE; NEUROECTODERM TUMOR; PRESCHOOL CHILD; PRIORITY JOURNAL; PROSTATE CANCER; SCHOOL CHILD; SCREENING TEST;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ADENOMATOUS POLYPOSIS COLI; ADRENAL CORTEX NEOPLASMS; ADULT; AGE OF ONSET; ATTITUDE TO HEALTH; CHILD; DATABASES, GENETIC; FEMALE; FORECASTING; GENETIC COUNSELING; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; GENOTYPE; HUMANS; LI-FRAUMENI SYNDROME; LOSS OF HETEROZYGOSITY; MOLECULAR SEQUENCE DATA; MUTATION; MUTS HOMOLOG 2 PROTEIN; NEOPLASM PROTEINS; PEDIGREE; PHENOTYPE; PREGNANCY; PRENATAL DIAGNOSIS; PROTEIN KINASES; TUMOR SUPPRESSOR PROTEIN P53; VON HIPPEL-LINDAU DISEASE;

EID: 77249085667     PISSN: 13899600     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10689-009-9245-9     Document Type: Article

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