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1 . Academic Journal
The history of families at-risk for hereditary breast and ovarian cancer: what are the impacts of genetic counseling and testing?
저자
by
Natalia Campacci
;
Rebeca Silveira Grasel
;
Henrique de Campos Reis Galvão
;
Lucas França Garcia
;
Paula Carvalho Ribeiro
, et al.
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Frontiers in Psychology, Vol 15 (2024)
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7 . Academic Journal
Exploring the frequency of a TP53 polyadenylation signal variant in tumor DNA from patients diagnosed with lung adenocarcinomas, sarcomas and uterine leiomyomas
저자
by
Igor Araujo Vieira
;
Guilherme Danielski Viola
;
Eduarda Heidrich Pezzi
;
Thayne Woycinck Kowalski
;
Bruna Vieira Fernandes
, et al.
소스
Genetics and Molecular Biology, Vol 46, Iss 3 suppl 1 (2024)
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7 . Academic Journal
New insights on familial colorectal cancer type X syndrome
저자
by
Felipe Antonio de Oliveira Garcia
;
Edilene Santos de Andrade
;
Henrique de Campos Reis Galvão
;
Cristina da Silva Sábato
;
Natália Campacci
, et al.
소스
Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
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7 . Academic Journal
Insights on variant analysis in silico tools for pathogenicity prediction
저자
by
Felipe Antonio de Oliveira Garcia
;
Edilene Santos de Andrade
;
Edenir Inez Palmero
.
소스
Frontiers in Genetics, Vol 13 (2022)
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5 . Academic Journal
Hereditary Breast Cancer in the Brazilian State of Ceará (The CHANCE Cohort): Higher-Than-Expected Prevalence of Recurrent Germline Pathogenic Variants
저자
by
Ana Carolina Leite Vieira Costa Gifoni
;
Markus Andret Cavalcante Gifoni
;
Camila Martins Wotroba
;
Edenir Inez Palmero
;
Eduardo Leite Vieira Costa
, et al.
소스
Frontiers in Oncology, Vol 12 (2022)
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7 . Academic Journal
Cost-Effectiveness of BRCA 1/2 Genetic Test and Preventive Strategies: Using Real-World Data From an Upper-Middle Income Country
저자
by
Marina Lourenção
;
Julia Simões Correa Galendi
;
Henrique de Campos Reis Galvão
;
Augusto Perazzolo Antoniazzi
;
Rebeca Silveira Grasel
, et al.
소스
Frontiers in Oncology, Vol 12 (2022)
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7 . Academic Journal
Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population
저자
by
Simone da Costa e Silva Carvalho
;
Nathalia Moreno Cury
;
Danielle Barbosa Brotto
;
Luiza Ferreira de Araujo
;
Reginaldo Cruz Alves Rosa
, et al.
소스
BMC Medical Genomics, Vol 13, Iss 1, Pp 1-24 (2020)
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7 . Academic Journal
miRNA expression profiling of hereditary breast tumors from BRCA1- and BRCA2-germline mutation carriers in Brazil
저자
by
Danielle Pessôa-Pereira
;
Adriane Feijó Evangelista
;
Rhafaela Lima Causin
;
René Aloisio da Costa Vieira
;
Lucas Faria Abrahão-Machado
, et al.
소스
BMC Cancer, Vol 20, Iss 1, Pp 1-10 (2020)
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7 . Academic Journal
Whole-Exome Sequencing Identifies Pathogenic Germline Variants in Patients with Lynch-Like Syndrome
저자
by
Wellington dos Santos
;
Edilene Santos de Andrade
;
Felipe Antonio de Oliveira Garcia
;
Natália Campacci
;
Cristina da Silva Sábato
, et al.
소스
Cancers, Vol 14, Iss 17, p 4233 (2022)
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7 . Academic Journal
Using Co-segregation and Loss of Heterozygosity Analysis to Define the Pathogenicity of Unclassified Variants in Hereditary Breast Cancer Patients
저자
by
Rebeca Silveira Grasel
;
Paula Silva Felicio
;
André Escremim de Paula
;
Natalia Campacci
;
Felipe Antônio de Oliveira Garcia
, et al.
소스
Frontiers in Oncology, Vol 10 (2020)
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