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Frontiers in Oncology
|
February 14, 2022
Novel Insights From the Germline Landscape of Breast Cancer in Brazil
Daniel Barbalho, Renata Sandoval, Erika Santos, et al.
The Lancet. Oncology
|
August 12, 2016
Brazilian health-care policy for targeted oncology therapies and companion diagnostic testing
Carlos Gil Ferreira, Maria Isabel Achatz, Patricia Ashton-Prolla, et al.
European Journal of Cancer (Oxford, England : 1990)
|
June 19, 2019
Reproductive factors associated with breast cancer risk in Li-Fraumeni syndrome
Payal P Khincha, Ana F Best, Joseph F Fraumeni, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 3, 2017
Clinical Management and Tumor Surveillance Recommendations of Inherited Mismatch Repair Deficiency in Childhood
Uri Tabori, Jordan R Hansford, Maria Isabel Achatz, et al.
Archives of Endocrinology and Metabolism
|
August 1, 2019
Pheochromocytoma and paraganglioma: implications of germline mutation investigation for treatment, screening, and surveillance
Ana Milena Gómez, Diogo Cordeiro Soares, Alexandre André Balieiro Costa, et al.
Frontiers in Genetics
|
February 19, 2021
Prevalence of the Brazilian <i>TP53</i> Founder c.1010G>A (p.Arg337His) in Lung Adenocarcinoma: Is Genotyping Warranted in All Brazilian Patients?
Igor Araujo Vieira, Tiago Finger Andreis, Bruna Vieira Fernandes, et al.
Familial Cancer
|
June 2, 2021
Utility of interim blood tests for cancer screening in Li-Fraumeni syndrome
Leatrisse Oba, Ana F Best, Phuong L Mai, et al.
Plos One
|
December 1, 2015
Ancestry of the Brazilian TP53 c.1010G>A (p.Arg337His, R337H) Founder Mutation: Clues from Haplotyping of Short Tandem Repeats on Chromosome 17p
Diego Davila Paskulin, Juliana Giacomazzi, Maria Isabel Achatz, et al.
Genes
|
August 26, 2023
Co-Occurrence of Germline Genomic Variants and Copy Number Variations in Hereditary Breast and Colorectal Cancer Patients
Luiza Côrtes, Tatiane Ramos Basso, Rolando André Rios Villacis, et al.
Oncotarget
|
April 14, 2017
HABP2 p.G534E variant in patients with family history of thyroid and breast cancer
Maisa Pinheiro, Sandra Aparecida Drigo, Renata Tonhosolo, et al.
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Search research articles
Search
Showing results (11-20 of 71) with videos related to
Sort By:
Page
of 8
Frontiers in Oncology
|
February 14, 2022
Novel Insights From the Germline Landscape of Breast Cancer in Brazil
Daniel Barbalho, Renata Sandoval, Erika Santos, et al.
The Lancet. Oncology
|
August 12, 2016
Brazilian health-care policy for targeted oncology therapies and companion diagnostic testing
Carlos Gil Ferreira, Maria Isabel Achatz, Patricia Ashton-Prolla, et al.
European Journal of Cancer (Oxford, England : 1990)
|
June 19, 2019
Reproductive factors associated with breast cancer risk in Li-Fraumeni syndrome
Payal P Khincha, Ana F Best, Joseph F Fraumeni, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 3, 2017
Clinical Management and Tumor Surveillance Recommendations of Inherited Mismatch Repair Deficiency in Childhood
Uri Tabori, Jordan R Hansford, Maria Isabel Achatz, et al.
Archives of Endocrinology and Metabolism
|
August 1, 2019
Pheochromocytoma and paraganglioma: implications of germline mutation investigation for treatment, screening, and surveillance
Ana Milena Gómez, Diogo Cordeiro Soares, Alexandre André Balieiro Costa, et al.
Frontiers in Genetics
|
February 19, 2021
Prevalence of the Brazilian <i>TP53</i> Founder c.1010G>A (p.Arg337His) in Lung Adenocarcinoma: Is Genotyping Warranted in All Brazilian Patients?
Igor Araujo Vieira, Tiago Finger Andreis, Bruna Vieira Fernandes, et al.
Familial Cancer
|
June 2, 2021
Utility of interim blood tests for cancer screening in Li-Fraumeni syndrome
Leatrisse Oba, Ana F Best, Phuong L Mai, et al.
Plos One
|
December 1, 2015
Ancestry of the Brazilian TP53 c.1010G>A (p.Arg337His, R337H) Founder Mutation: Clues from Haplotyping of Short Tandem Repeats on Chromosome 17p
Diego Davila Paskulin, Juliana Giacomazzi, Maria Isabel Achatz, et al.
Genes
|
August 26, 2023
Co-Occurrence of Germline Genomic Variants and Copy Number Variations in Hereditary Breast and Colorectal Cancer Patients
Luiza Côrtes, Tatiane Ramos Basso, Rolando André Rios Villacis, et al.
Oncotarget
|
April 14, 2017
HABP2 p.G534E variant in patients with family history of thyroid and breast cancer
Maisa Pinheiro, Sandra Aparecida Drigo, Renata Tonhosolo, et al.
Page
of 8