Is the controversy on breast cancer as part of the Lynch-related tumor spectrum still open?

Familial Cancer

Volumn 11, Issue 4, 2012, Pages 681-683

  Grandval, Philippe ^a,b   Barouk Simonet, Emmanuelle ^c   Bronner, Myriam ^d   Buisine, Marie Pierre ^e   Moretta, Jessica ^f   Tinat, Julie ^g   Olschwang, Sylviane ^a,b,h,i  

^a AIX MARSEILLE UNIVERSITY   (France)

^b TIMONE HOSPITAL   (France)

^c INSTITUT BERGONIÉ   (France)

^d CHU NANCY BRABOIS   (France)

^e LILLE UNIVERSITY HOSPITAL   (France)

^f INSTITUT PAOLI CALMETTES   (France)

^g ROUEN UNIVERSITY HOSPITAL   (France)

^h Hospital Ambroise Pare   (France)

ⁱ Departement Genetique Medicale   (France)

Author keywords

Cancer risk; Lynch syndrome; MSI type; Mutation carrier; Screening guidelines

Indexed keywords

ADULT; AGED; ARTICLE; BREAST ADENOCARCINOMA; BREAST CANCER; CANCER RISK; CANCER SCREENING; CANCER SUSCEPTIBILITY; CLINICAL ARTICLE; GENE MUTATION; GENETIC PREDISPOSITION; GENOTYPE; GERM LINE; HEREDITARY NONPOLYPOSIS COLORECTAL CANCER; HETEROZYGOTE; HIGH RISK PATIENT; HUMAN; HYPOTHESIS; LOSS OF FUNCTION MUTATION; MISMATCH REPAIR; NUCLEOTIDE SEQUENCE; PANCREAS ADENOCARCINOMA; PANCREAS CANCER; PRACTICE GUIDELINE; PRIORITY JOURNAL; RISK FACTOR;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; BREAST NEOPLASMS; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; DNA MISMATCH REPAIR; FEMALE; GERM-LINE MUTATION; HUMANS; IMMUNOENZYME TECHNIQUES; MICROSATELLITE INSTABILITY; MUTS HOMOLOG 2 PROTEIN; NUCLEAR PROTEINS; PANCREATIC NEOPLASMS; PROGNOSIS;

EID: 84870409260     PISSN: 13899600     EISSN: 15737292     Source Type: Journal    
DOI: 10.1007/s10689-012-9562-2     Document Type: Article

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