المؤلفون: Tom van Wezel, Amine Elghali, Hans Morreau, Mohamed Msaddak Azzouz, Karim Skandrani, Mehdi ksiaa, Rihab Ben Sghaier, Rached Ltaief, Ali Saad, Slim Ben Ahmed, Fahmi Hmila, Fathi Darbel, Olfa Hellara, Moncef Mokkni, Ameni Gdissa, Anne M.L. Jansen, Moez Gribaa, Leila Ben Fatma, Ahlem Bdioui, Lamia Elgolli

المصدر: Familial Cancer, 18(3), 343-348. SPRINGER

مصطلحات موضوعية: Male, 0301 basic medicine, Oncology, Cancer Research, 030105 genetics & heredity, Immunohistochemical staining, Germline, Loss of heterozygosity, 0302 clinical medicine, MMR panel, Family history, Poly-ADP-Ribose Binding Proteins, Genetics (clinical), Sanger sequencing, Tumor, High-Throughput Nucleotide Sequencing, Middle Aged, Lynch syndrome, Pedigree, MutS Homolog 2 Protein, 030220 oncology & carcinogenesis, symbols, Female, DNA mismatch repair genes, Colorectal Neoplasms, MutL Protein Homolog 1, Adult, Heterozygote, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Tunisia, Young Adult, 03 medical and health sciences, symbols.namesake, Internal medicine, Genetics, medicine, Genetic predisposition, Humans, neoplasms, Germ-Line Mutation, Aged, DNA Polymerase III, Family Health, POLD1, business.industry, DNA Polymerase II, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, MSH2, business, Gene Deletion

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::575b8ee0db82ac75c4c007e578c940aa
https://hdl.handle.net/1887/121808