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Frontiers in Oncology, ISSN 2234-943X, 07/2018, Volume 8, p. 259
Liquid biopsies are increasingly used in the care of patients with advanced cancers. These tests are used to find mutations and other genomic alterations,... 
Cell-free DNA | Germline mutation | Liquid biopsy | Hereditary cancer syndromes | Pancreaticobiliary neoplasms | CLINICAL-ONCOLOGY | PREVALENCE | BRCA2 | germline mutation | BREAST-CANCER | ONCOLOGY | hereditary cancer syndromes | cell-free DNA | UPDATE | MUTATIONS | POLICY STATEMENT | TUMOR DNA | liquid biopsy | pancreaticobiliary neoplasms | AMERICAN-SOCIETY
Journal Article
Cancer, ISSN 0008-543X, 11/2017, Volume 123, Issue 22, pp. 4363 - 4371
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2017, Volume 35, Issue 15_suppl, pp. e13109 - e13109
Journal Article
Journal of Urology, The, ISSN 0022-5347, 2017, Volume 197, Issue 4, pp. e423 - e423
Journal Article
Journal of Urology, The, ISSN 0022-5347, 2017, Volume 197, Issue 4, pp. e501 - e501
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 02/2017, Volume 35, Issue 6_suppl, pp. 85 - 85
85 Background: Prostate cancer (PC) has been associated with germline mutations in several genes, most often BRCA2. Recently, 11.8% of men with metastatic PC... 
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 02/2017, Volume 35, Issue 4_suppl, pp. 537 - 537
537 Background: Approximately 5-10% of colorectal cancer (CRC) is due to hereditary causes. Identification of an inherited cause may impact surgical and... 
Journal Article
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 2, pp. 107 - 115
Journal Article
Molecular Diagnosis and Therapy, ISSN 1177-1062, 02/2013, Volume 17, Issue 1, pp. 31 - 47
Prevalent as an acquired abnormality in cancer, the role of tumor protein p53 (TP53) as a germline mutation continues to evolve. The clinical impact of a... 
BREAST-CANCER | MAMMOGRAPHIC DENSITY | GENETICS & HEREDITY | GERMLINE MUTATIONS | MUTANT P53 | MYELOGENOUS LEUKEMIA | CHRONIC LYMPHOCYTIC-LEUKEMIA | PHARMACOLOGY & PHARMACY | PREDICTIVE-VALUE | CHOROID-PLEXUS TUMORS | SOFT-TISSUE-SARCOMA | OLIGONUCLEOTIDE OLP53 | Breast cancer | Mutation | Genes | Tumors
Journal Article
International journal of clinical medicine, ISSN 2158-284X, 12/2012, Volume 3, Issue 7, pp. 607 - 613
Deleterious mutations in the gene cause hereditary leukemia due to a rare syndrome called Familial platelet Disorder with Associated Myeloid Malignancy... 
eczema | L472X | hereditary leukemia | RUNX1c isoform | FPDMM
Journal Article
International Journal of Clinical Medicine, ISSN 2158-284X, 12/2012, Volume 3, Issue 7, pp. 607 - 607
Deleterious mutations in the RUNX1 gene cause hereditary leukemia due to a rare syndrome called Familial platelet Disorder with Associated Myeloid Malignancy... 
Journal Article
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