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Cancer syndrome
Fanconi Anemia: Guidelines for Diagnosis and Management
Review of Cancer Genetics
Hereditary Breast and Ovarian Cancer Syndrome
Homologous Recombination Deficiency: Exploiting the Fundamental Vulnerability of Ovarian Cancer
Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients
Ovarian Cancer Causes, Risk Factors, and Prevention Risk Factors
Ovarian Cancer Genetics
Oral Cancer-Related Inherited Cancer Syndromes: a Comprehensive Review 1Gargi S Sarode, 2Akshit Batra, 3Sachin C Sarode, 4Sujata Yerawadekar, 5Shankargouda Patil
ACOG: Practice Bulletin for Hereditary Breast and Ovarian Cancer
Blueprint Genetics Fanconi Anemia Panel
Review DNA Mismatch Repair Genes and Colorectal Cancer
Comprehensive Inherited Cancer Precision Panel Overview
Hereditary Prostate Cancer
NCCN Guidelines®) Genetic/Familial High-Risk Assessment: Colorectal
BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer Syndrome
Prevalence of Germline Pathogenic Variants in Cancer Predisposing Genes in Czech and Belgian Pancreatic Cancer Patients
Constitutional Mismatch Repair Deficiency Syndrome
Hereditary Breast and Ovarian Cancer Syndrome (HBOC): BRCA1 and BRCA2 Mutations
Top View
Breast Cancer
Lynch Syndrome–Associated Breast Cancers: Clinicopathologic Characteristics of a Case Series from the Colon Cancer Family Registry
NCCN: Genetic/Familial High-Risk Assessment: Breast and Ovarian
Biallelic Truncating FANCM Mutations Cause Early-Onset Cancer but Not Fanconi Anemia
Cancer Can Run in the Family
CANCER GENOMICS BEST PRACTICES for Connecticut Healthcare Providers
Cancer Susceptibility Mutations in Patients with Urothelial Malignancies the Following Represents Disclosure Information Provided by Authors of This Manuscript
Diagnosis of Lynch Syndrome and Strategies to Distinguish Lynch-Related Tumors from Sporadic MSI/Dmmr Tumors
Immune Activation in Mismatch Repair–Deficient Carcinogenesis: More Than Just Mutational Rate Jason A
The Role of Hereditary Nonpolyposis Colorectal Cancer in the Management of Familial Ovarian Cancer
Blueprint Genetics Comprehensive Hereditary Cancer Panel
Familial/Inherited Cancer Syndrome: a Focus on the Highly Consanguineous Arab Population
Cancer Is Not Just One Disease Cancer and Genetics Gene
Prevalence of Germline Mutations in Cancer Susceptibility Genes In
Testing for Hereditary Breast and Ovarian Cancer Syndrome
Evaluation of Colorectal Cancers for Lynch Syndrome: Practical Molecular Diagnostics for Surgical Pathologists Wade S Samowitz
Hereditary Cancer Syndrome Multigene Panels
Hereditary Ovarian Cancer
MLH1-Rhemac Hereditary Nonpolyposis Colorectal Cancer Syndrome in Rhesus Macaques
About MSH2 Gene Mutations About Genes MSH2 Mutations and Cancer Risk Genes Are in Every Cell in Our Bodies
Family Cancer Syndromes
Information for Patients and Their Families
WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family
Lynch Syndrome: Its Impact on Urothelial Carcinoma
Alteration of DNA Mismatch Repair Capacity Underlying the Co-Occurrence of Non-Small-Cell Lung Cancer and Nonmedullary Thyroid C
Hereditary Cancer Risk Assessment for Gynecological Cancers
Identification of Cancer Patients with Lynch Syndrome: Clinically Significant Discordances and Problems in Tissue-Based Mismatch Repair Testing
Hereditary Cancer Syndrome Multigene Panels
Genetic Testing for Hereditary Cancer – Commercial Medical Policy
A Case Report of Germline Compound Heterozygous Mutations in the BRCA1 Gene of an Ovarian and Breast Cancer Patient
Targeting DNA Repair and Chromatin Crosstalk in Cancer Therapy
Familial Cancer Syndromes
Inhibition of DNA Repair in Cancer Therapy: Toward a Multi-Target Approach
Hereditary Breast and Ovarian Cancer Syndrome: Looking for Mutations in ERCC4 When Brcas Are Not the Origin
Cancer Risks Associated with Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch Syndrome
The Coding Region of the Bloom Syndrome BLM Gene and of the CBL Proto-Oncogene Is Mutated in Genetically Unstable Sporadic Gastrointestinal Tumors1
Genetic Causes of Cancer Predisposition in Children and Adolescents
Fanconi Anemia Precision Panel Overview Indications Clinical Utility
Highly Penetrant Hereditary Cancer Syndromes
Gynecological Cancers Caused by Deficient Mismatch Repair
Colon Cancer and Lynch Syndrome
BRCA1 Gene BRCA1, DNA Repair Associated
About MLH1 Gene Mutations About Genes MLH1 Mutations and Cancer Risk Genes Are in Every Cell in Our Bodies