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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 -
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المؤلفون: Guy Van Camp, Jean-Pierre Renard, Paul Coucke, Jan Hellemans, Dieter Deforce, Jo Vandesompele, Steve Lefever, Joachim De Schrijver, Wim Van Criekinge, Hendrik Van de Voorde, Filip Pattyn, Sarah De Keulenaer, Daisy Flamez, Mohammad Amin Tabatabaiefar, Bieke Scharlaken, Filip Van Nieuwerburgh, Sofie Bekaert
المصدر: BMC MEDICAL GENOMICS
BMC Medical Genomics, Vol 5, Iss 1, p 17 (2012)
BMC Medical Genomicsمصطلحات موضوعية: lcsh:Internal medicine, lcsh:QH426-470, Hearing loss, Genetic diagnostics, Biology, Deafness, Congenital hearing loss, Polymerase Chain Reaction, PCR based enrichment, Connexins, symbols.namesake, Next generation sequencing, Genetics, medicine, OTOF, otorhinolaryngologic diseases, Humans, Genetics(clinical), lcsh:RC31-1245, Genetics (clinical), Sanger sequencing, MUTATIONS, High-Throughput Nucleotide Sequencing, Biology and Life Sciences, Amplicon, IMPAIRMENT, Molecular diagnostics, Human genetics, Connexin 26, lcsh:Genetics, Molecular Diagnostic Techniques, Mutation (genetic algorithm), symbols, Human medicine, medicine.symptom, Research Article
وصف الملف: application/pdf; pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34fa53bcb0817090c655f418eed5771cTest
https://biblio.ugent.be/publication/3070495/file/3070512Test -
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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