Prevalence of the BRCA1 founder mutation c.5266dupin Brazilian individuals at-risk for the hereditary breast and ovarian cancer syndrome

Hereditary Cancer in Clinical Practice

Volumn 9, Issue 1, 2011, Pages

  Ewald, Ingrid P ^a,b   Izetti, Patrícia ^a,b   Vargas, Fernando R ^c,d   Moreira, Miguel A M ^d,e   Moreira, Aline S ^d,e   Moreira Filho, Carlos A ^f   Cunha, Danielle R ^g   Hamaguchi, Sara ^g   Camey, Suzi A ^b   Schmidt, Aishameriane ^b   Caleffi, Maira ^h   Koehler Santos, Patrícia ^a,b   Giugliani, Roberto ^a,b   Ashton Prolla, Patricia ^a,b  

^a HOSPITAL DE CLÍNICAS DE PORTO ALEGRE   (Brazil)

^b FEDERAL UNIVERSITY OF RIO GRANDE DO SUL   (Brazil)

^c FEDERAL UNIVERSITY OF THE STATE OF RIO DE JANEIRO   (Brazil)

^d INSTITUTO NACIONAL DE CÂNCER   (Brazil)

^e INSTITUTO OSWALDO CRUZ   (Brazil)

^f UNIVERSITY OF SÃO PAULO   (Brazil)

^g HOSPITAL ISRAELITA ALBERT EINSTEIN   (Brazil)

^h HOSPITAL MOINHOS DE VENTO   (Brazil)

Author keywords

BRCA1 gene; BRCA2 gene; Founder mutations; Hereditary breast and ovarian cancer syndrome; Hereditary breast cancer

Indexed keywords

BRCA1 PROTEIN;

ADULT; AGED; ARTICLE; BRAZIL; CANCER RISK; FAMILY HISTORY; FEMALE; GENE DELETION; GENE FREQUENCY; GENE IDENTIFICATION; GENE MUTATION; GENETIC RISK; GENETIC SCREENING; HEREDITARY BREAST AND OVARIAN CANCER SYNDROME; HEREDITARY COLORECTAL CANCER; HEREDITARY NONPOLYPOSIS COLORECTAL CANCER; HIGH RISK PATIENT; HUMAN; MAJOR CLINICAL STUDY; MALE;

EID: 84862153329     PISSN: 17312302     EISSN: 18974287     Source Type: Journal    
DOI: 10.1186/1897-4287-9-12     Document Type: Article

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