المؤلفون: Kris Laukens, Joachim De Schrijver, Amélie Dendooven, Benedicte Y. De Winter, Els M. Gielis, Daniel Abramowicz, Marie-Paule Emonds, Wim Van Biesen, Pieter Meysman, Jean-Louis Bosmans, Steven Van Laecke, Kristien J. Ledeganck, Charlie Beirnaert, Jurgen Del Favero

المصدر: Nephrology, dialysis, transplantation

مصطلحات موضوعية: Adult, Graft Rejection, Male, medicine.medical_specialty, Adolescent, 030232 urology & nephrology, Urology, 030230 surgery, 03 medical and health sciences, chemistry.chemical_compound, Young Adult, 0302 clinical medicine, Postoperative Complications, Multiplex polymerase chain reaction, medicine, Humans, Longitudinal Studies, Kidney transplantation, Acute tubular necrosis, Aged, Computer. Automation, Transplantation, Creatinine, Kidney, business.industry, Graft Survival, Area under the curve, Middle Aged, medicine.disease, Prognosis, Kidney Transplantation, Tissue Donors, Survival Rate, medicine.anatomical_structure, chemistry, Cell-free fetal DNA, ROC Curve, Nephrology, Female, Kidney Diseases, Human medicine, business, Cell-Free Nucleic Acids, Biomarkers

وصف الملف: Print; pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b125df7690f42a5f752933b0d42b089fTest
https://lirias.kuleuven.be/handle/123456789/658855Test

المؤلفون: Hal Dietz, Ronald V. Lacro, Julie De Backer, Bart Loeys, Machteld Baetens, Joachim De Schrijver, Hendrik Van de Voorde, B Menten, Kim De Leeneer, Anne De Paepe, Paul Coucke, Jan Hellemans, Lut Van Laer, Wim Van Criekinge, Marjolijn Renard

المصدر: Human mutation

مصطلحات موضوعية: musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, DNA Mutational Analysis, Pilot Projects, Biology, Polymerase Chain Reaction, DNA sequencing, Marfan Syndrome, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, Multiplex polymerase chain reaction, Genetics, Humans, Missense mutation, Multiplex, Multiplex ligation-dependent probe amplification, Genetics (clinical), DNA Primers, 030304 developmental biology, Sanger sequencing, Loeys-Dietz Syndrome, 0303 health sciences, Polymorphism, Genetic, Massive parallel sequencing, Base Sequence, High-Throughput Nucleotide Sequencing, Reproducibility of Results, Molecular Diagnostic Techniques, Mutation, Mutation (genetic algorithm), symbols, Human medicine, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a68d871619bd6f4848a07c3ccfc4b646Test
https://hdl.handle.net/10067/920890151162165141Test

المؤلفون: Anne De Paepe, Jan Hellemans, Joachim De Schrijver, Wim Van Criekinge, Kathleen Claes, Bruce Poppe, Kim De Leeneer, Machteld Baetens, Paul Coucke

المساهمون: Center for Medical Genetics [Ghent], Ghent University Hospital, Laboratory for Bioinformatics and Computational Genomics, Ghent University, Universiteit Gent = Ghent University [Belgium] (UGENT)

المصدر: Human Mutation
Human Mutation, Wiley, 2011, 32 (3), pp.335. ⟨10.1002/humu.21428⟩

مصطلحات موضوعية: Cancer genome sequencing, DNA Mutational Analysis, Genes, BRCA2, Genes, BRCA1, Breast Neoplasms, Biology, Genome, Sensitivity and Specificity, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, Humans, Multiplex, Genetic Predisposition to Disease, Genetic Testing, Genetics (clinical), Illumina dye sequencing, Exome sequencing, 030304 developmental biology, Genetic testing, BRCA2 Protein, 0303 health sciences, Massive parallel sequencing, medicine.diagnostic_test, Base Sequence, BRCA1 Protein, Life Sciences, High-Throughput Nucleotide Sequencing, Sequence Analysis, DNA, 3. Good health, High-Throughput Screening Assays, 030220 oncology & carcinogenesis, Pyrosequencing, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcc1126202ac2eb8441e2988d9017cb4Test
https://pubmed.ncbi.nlm.nih.gov/21305653Test