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المؤلفون: Lies H. Hoefsloot, P. Martin van Hagen, L. Ingeborgh van den Born, Carel B. Hoyng, Kornelia Neveling, Frans P.M. Cremers, Mieke Kipping-Geertsema, Anna M. Siemiatkowska, Anneke I. den Hollander, Rob W.J. Collin, Monique Stoffels, Anna Simon, Arjen Henkes
المساهمون: Immunology, Ophthalmology
المصدر: Ophthalmology, 120, 2697-705
Ophthalmology, 120(12), 2697-2705. Elsevier Inc.
Ophthalmology, 120, 12, pp. 2697-705مصطلحات موضوعية: Adult, Male, Proband, Oncology, medicine.medical_specialty, Pathology, Genetics and epigenetic pathways of disease [NCMLS 6], DNA Mutational Analysis, Visual Acuity, Mevalonic Acid, Compound heterozygosity, Genomic disorders and inherited multi-system disorders [IGMD 3], Evaluation of complex medical interventions Genomic disorders and inherited multi-system disorders [NCEBP 2], Internal medicine, Retinitis pigmentosa, Electroretinography, medicine, Humans, Exome, Fluorescein Angiography, Exome sequencing, Mevalonate kinase deficiency, biology, business.industry, Genetic heterogeneity, Mevalonate kinase, Middle Aged, medicine.disease, Pedigree, Pathogenesis and modulation of inflammation [N4i 1], Phosphotransferases (Alcohol Group Acceptor), Ophthalmology, Mutation, biology.protein, Female, Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6], business, Retinitis Pigmentosa, Tomography, Optical Coherence
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b23a34004ac4b791b1b83b121055c17Test
https://doi.org/10.1016/j.ophtha.2013.07.052Test -
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المؤلفون: Hannes Helgason, Asbjorg Geirsdottir, Unnur Thorsteinsdottir, Haraldur Sigurdsson, Yaojun Song, Yaou Duan, G. Bragi Walters, Johannes P. H. van de Ven, Hongrong Luo, Tina Ristau, Frederieke E. Schoenmaker-Koller, Kang Zhang, Carel B. Hoyng, Ling Zhao, Paul S. Bernstein, Lambertus A. Kiemeney, Shirrina Patel, Camiel J. F. Boon, Sascha Fauser, Hreinn Stefansson, Olafur T. Magnusson, Gudleif Helgadottir, Gisli Masson, Kari Stefansson, Patrick Sulem, Ingileif Jonsdottir, Michelle Pei, Henry Ferreyra, Einar Stefánsson, Fridbert Jonasson, Thorunn Rafnar, Sandra Liakopoulos, Daniel F. Gudbjartsson, Anneke I. den Hollander, Gudmar Thorleifsson, Maheswara R Duvvari, Augustine Kong
المصدر: Nature Genetics, 45, 1371-4
Nature Genetics, 45, 11, pp. 1371-4
Nature Genetics, 45(11), 1371-U153مصطلحات موضوعية: Risk, Nonsynonymous substitution, medicine.medical_specialty, Genotype, Iceland, Aetiology, screening and detection [ONCOL 5], Complement factor I, Biology, Bioinformatics, Polymorphism, Single Nucleotide, Genomic disorders and inherited multi-system disorders [IGMD 3], Macular Degeneration, Gene Frequency, Evaluation of complex medical interventions Genomic disorders and inherited multi-system disorders [NCEBP 2], Molecular genetics, Genetic variation, Genetics, medicine, Humans, Genetic Predisposition to Disease, Allele, Complement Activation, Molecular epidemiology Aetiology, screening and detection [NCEBP 1], Sequence (medicine), Base Sequence, Genetic Variation, Complement C3, Sequence Analysis, DNA, Macular degeneration, medicine.disease, Amino Acid Substitution, Complement Factor H, Complement C3b, Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6], Genome-Wide Association Study
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a384c0fcdb1e74be68da544ed189cccTest
https://doi.org/10.1038/ng.2740Test -
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المؤلفون: Ad R. M. M. Hermus, K. Freriks, Hanneke Mieloo, Maaike A.F. Traas, Henri J L M Timmers, Dominique Smeets, Romana T. Netea-Maier, Janiëlle A E M van Alfen-van der Velden, Barto J. Otten, Catharina C. M. Beerendonk, Guillaume van de Zande, Lies H. Hoefsloot
المصدر: European Journal of Medical Genetics, 56, 9, pp. 497-501
European Journal of Medical Genetics, 56, 497-501مصطلحات موضوعية: Adult, Monosomy, Pathology, medicine.medical_specialty, Buccal swab, Turner Syndrome, Gonadoblastoma, Biology, Real-Time Polymerase Chain Reaction, Y chromosome, Genomic disorders and inherited multi-system disorders [IGMD 3], Turner syndrome, Tissue mosaicism, Genetics, medicine, Humans, Hormonal regulation Translational research [IGMD 6], Genetic Predisposition to Disease, Lymphocytes, In Situ Hybridization, Fluorescence, Genetics (clinical), X chromosome, Ovarian Neoplasms, Chromosomes, Human, X, Chromosomes, Human, Y, Mosaicism, Hormonal regulation [IGMD 6], Mouth Mucosa, Karyotype, General Medicine, medicine.disease, Human Reproduction [NCEBP 12], Female, Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6]
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::116177bcd37fd78bae5eb92f1fd873efTest
https://doi.org/10.1016/j.ejmg.2013.07.008Test -
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المؤلفون: Arjan P.M. de Brouwer, Angel Ashikov, Rita Gerardy-Schahn, Samuel Schmidt, Joris H. Robben, Miski Mohamed, Maïlys Guillard, Ron A. Wevers, B. van den Heuvel, Peter M.T. Deen, Eva Morava, Dirk Lefeber
المصدر: Neurology, 81, 7, pp. 681-7
Neurology, 81, 681-7مصطلحات موضوعية: Male, Chemical and physical biology [NCMLS 7], medicine.medical_specialty, Glycosylation, Ataxia, Adolescent, Genomic disorders and inherited multi-system disorders Energy and redox metabolism [IGMD 3], DCN MP - Plasticity and memory, Blotting, Western, DNA Mutational Analysis, Mutant, Mutation, Missense, Biology, Hemorrhagic Disorders, medicine.disease_cause, Polymorphism, Single Nucleotide, Renal disorder Energy and redox metabolism [IGMD 9], Abnormal protein glycosylation, Genomic disorders and inherited multi-system disorders [IGMD 3], Young Adult, Intellectual Disability, Internal medicine, medicine, Humans, Missense mutation, Child, Glycostation disorders [DCN PAC - Perception action and control IGMD 4], DCN NN - Brain networks and neuronal communication, Genetics, Mutation, Mitochondrial medicine Energy and redox metabolism [IGMD 8], Glycostation disorders [IGMD 4], medicine.disease, Disease gene identification, Pedigree, Genetics and epigenetic pathways of disease DCN MP - Plasticity and memory [NCMLS 6], Renal disorder Membrane transport and intracellular motility [IGMD 9], carbohydrates (lipids), Bleeding diathesis, Membrane transport and intracellular motility Renal disorder [NCMLS 5], Endocrinology, Cytidine Monophosphate N-Acetylneuraminic Acid, Nucleotide Transport Proteins, Mutation testing, Female, Neurology (clinical), medicine.symptom
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bd2210be2243f322d3a0fb594dd4238Test
https://doi.org/10.1212/wnl.0b013e3182a08f53Test -
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المؤلفون: Arjen R. Mensenkamp, Ron A. Wevers, Jyotsna U. Rao, Angelina G. Goudswaard, Henricus P.M. Kunst, Udo F. H. Engelke, Karel Pacak, Graeme Eisenhofer, Nan Qin, Ad Hermus, Jacques W. M. Lenders, Richard J. Rodenburg, Henri J. L. M. Timmers, Benno Kusters, Fred C.G.J. Sweep
المصدر: Clinical Cancer Research; Vol 19
Clinical Cancer Research, 19, 3787-95
Clinical Cancer Research, 19, 14, pp. 3787-95مصطلحات موضوعية: Male, Cancer Research, SDHB, Adrenal Gland Neoplasms, Succinic Acid, DCN PAC - Perception action and control, Mitochondrion, Catecholamines, 0302 clinical medicine, Paraganglioma, Citrate synthase, 0303 health sciences, Cardiovascular diseases [NCEBP 14], Electron Transport Complex II, Succinate dehydrogenase, Middle Aged, Mitochondria, 3. Good health, Mitochondrial medicine [IGMD 8], Oncology, 030220 oncology & carcinogenesis, Female, medicine.drug, Adult, medicine.medical_specialty, Adolescent, Genotype, Pheochromocytoma, Biology, Article, Genomic disorders and inherited multi-system disorders [IGMD 3], Young Adult, 03 medical and health sciences, Internal medicine, ONCOL 3 - Translational research DCN MP - Plasticity and memory, medicine, Humans, Glycostation disorders [DCN PAC - Perception action and control IGMD 4], DCN NN - Brain networks and neuronal communication, 030304 developmental biology, Translational research Genomic disorders and inherited multi-system disorders [ONCOL 3], Hormonal regulation [IGMD 6], Glycostation disorders [IGMD 4], medicine.disease, Endocrinology, Hereditary cancer and cancer-related syndromes Genomic disorders and inherited multi-system disorders [ONCOL 1], biology.protein, Catecholamine, Hormonal regulation Aetiology, screening and detection [IGMD 6], SDHD, Energy Metabolism
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a8b55612d5f34a85347800592c9f568Test
https://doi.org/10.1158/1078-0432.ccr-12-3922Test -
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المؤلفون: S. H. Powis, Robert Kleta, Marieke J H Coenen, Anne Boland-Augé, Peter W. Mathieson, Paul Brenchley, Hanna Debiec, Jack F.M. Wetzels, Johanne M. Groothuismink, Bénédicte Stengel, Horia Stanescu, Alan Medlar, Julia M. Hofstra, Pierre Ronco, Detlef Bockenhauer
المساهمون: Department of Human Genetics [Nijmegen], Radboud University Medical Center [Nijmegen], Department of Nephrology [Nijmegen, The Netherlands], Des Maladies Rénales Rares aux Maladies Fréquentes, Remodelage et Réparation, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), CHU Tenon [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Centre for Nephrology [London, UK], University College of London [London] (UCL), Centre de recherche en épidémiologie et santé des populations (CESP), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Université Paris-Sud - Paris 11 (UP11)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre National de Génotypage (CNG), Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Academic Renal Unit [Bristol, UK], University of Bristol [Bristol], School of Biomedicine [Manchester, UK], University of Manchester [Manchester], The research leading to these results has received funding from the European Community’s Seventh Framework Programme under grant agreement 2012-305608 'European Consortium for High-Throughput Research in Rare Kidney Diseases' (EURenOmics)' (to P.W.M., P.E.B., R.K., J.F.M.W., P.R.), by the David and Elaine Potter Charitable Foundation (to S.H.P., R.K.), by the Dutch Kidney Foundation (J.M.H., grant KJPB11.021), and by the FrenchFoundation for Medical Research (H.D., P.R., grant 2012). The French Gn-Progress cohort was supported by grants from the French Ministry of Health (PHRC AOM 00022), the Ministry of Research (Decision d’aide 01P0513), and the Biomedicine Agency (AO Recherche et Greffes 2005)., Department of Human Genetics, Department of nephrology, Remodelage et Reparation du Tissu Renal, Centre for Nephrology, Equipe 10, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris-Sud - Paris 11 (UP11)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris-Sud - Paris 11 (UP11)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Academic Renal Unit, School of Biomedicine, Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), The research leading to these results has received funding from the European Community's Seventh Framework Programme under grant agreement 2012-305608 'European Consortium for High-Throughput Research in Rare Kidney Diseases' (EURenOmics)'(to P.W.M., P.E.B., R.K., J.F.M.W., P.R.), by the David and Elaine Potter Charitable Foundation (to S.H.P., R.K.), by the Dutch Kidney Foundation (J.M.H., grant KJPB11.021), and by the French Foundation for Medical Research (H.D., P.R., grant 2012). The French Gn-Progress cohort was supported by grants from the French Ministry of Health (PHRC AOM 00022), the Ministry of Research (Decision d'aide 01P0513), and the Biomedicine Agency (AO Recherche et Greffes 2005)., RONCO, Pierre, Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Université Paris-Sud - Paris 11 (UP11)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Université Paris-Sud - Paris 11 (UP11)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM), Service de Département de Néphrologie = Service de Néphrologie et Dialyses [CHU Tenon], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Radboud University Medical Centre [Nijmegen, The Netherlands], Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC), Service de Néphrologie et Dialyses [CHU Tenon], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Tenon [AP-HP], Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris-Sud - Paris 11 (UP11)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)
المصدر: Journal of the American Society of Nephrology
Journal of the American Society of Nephrology, 2013, 24 (4), pp.677-683. ⟨10.1681/ASN.2012070730⟩
Journal of the American Society of Nephrology, American Society of Nephrology, 2013, 24 (4), pp.677-83. ⟨10.1681/ASN.2012070730⟩
Journal of the American Society of Nephrology, 2013, 24 (4), pp.677-83. ⟨10.1681/ASN.2012070730⟩
Journal of the American Society of Nephrology, American Society of Nephrology, 2013, 24 (4), pp.677-683. ⟨10.1681/ASN.2012070730⟩
Journal of the American Society of Nephrology, 24, 4, pp. 677-83
Journal of the American Society of Nephrology; Vol 24
Journal of the American Society of Nephrology, 24, 677-83مصطلحات موضوعية: Male, MESH: Sequence Analysis, DNA, MESH: Glomerulonephritis, Membranous, 030232 urology & nephrology, Glomerulonephritis, Membranous, Exon, 0302 clinical medicine, Coding region, MESH: Genomic Structural Variation, Renal disorder [IGMD 9], MESH: Aged, Genetics, Sanger sequencing, 0303 health sciences, MESH: Middle Aged, MESH: Polymorphism, Single Nucleotide, MESH: Genetic Predisposition to Disease, General Medicine, Middle Aged, 3. Good health, Nephrology, symbols, [SDV.BBM.GTP] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], Female, Adult, dbSNP, Sequence analysis, Biology, Polymorphism, Single Nucleotide, Mental health [NCEBP 9], Genomic disorders and inherited multi-system disorders [IGMD 3], 03 medical and health sciences, symbols.namesake, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], MESH: Receptors, Phospholipase A2, Humans, Genetic Predisposition to Disease, Allele, 1000 Genomes Project, Genomic disorders and inherited multi-system disorders Molecular epidemiology [IGMD 3], Gene, Aged, 030304 developmental biology, MESH: Humans, Receptors, Phospholipase A2, MESH: Adult, Sequence Analysis, DNA, Molecular biology, MESH: Male, Genomic Structural Variation, MESH: Female
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b192b20a06677d3bf650e3bd66ad35fTest
https://doi.org/10.1681/asn.2012070730Test -
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المؤلفون: Carlo Marcelis, Rolph Pfundt, Bart C.W. Kuipers, Bert B.A. de Vries, Nicole de Leeuw, Anneke T. Vulto-van Silfhout
المصدر: Clinical Dysmorphology, 22, 1, pp. 18-21
Clinical Dysmorphology, 22, 18-21مصطلحات موضوعية: Male, Candidate gene, Prominent forehead, Haploinsufficiency, GPI-Linked Proteins, Pathology and Forensic Medicine, Genomic disorders and inherited multi-system disorders DCN MP - Plasticity and memory [IGMD 3], Genomic disorders and inherited multi-system disorders [IGMD 3], Intellectual Disability, Intellectual disability, medicine, Humans, Abnormalities, Multiple, Short philtrum, Dysmorphic facial features, Genetics (clinical), Oligonucleotide Array Sequence Analysis, Genetics, business.industry, Neuropeptides, Infant, General Medicine, medicine.disease, Genetics and epigenetic pathways of disease DCN MP - Plasticity and memory [NCMLS 6], DNA-Binding Proteins, Feeding problems, Facial Asymmetry, Child, Preschool, Pediatrics, Perinatology and Child Health, Chromosomes, Human, Pair 6, Female, Syndactyly, Anatomy, Chromosome Deletion, business, Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6], Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e8c255dfe5b4731ba8b6b01e58a866eTest
https://doi.org/10.1097/mcd.0b013e32835b6e39Test -
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المؤلفون: Roosing, S., Rohrschneider, K., Beryozkin, A., Sharon, D., Weisschuh, N., Staller, J., Kohl, S., Zelinger, L., Peters, T.A., Neveling, K., Strom, T.M., Disease, C. European Retina, Born, L.I. van den, Hoyng, C.B., Klaver, C.C., Roepman, R., Wissinger, B., Banin, E., Cremers, F.P.M., Hollander, A.I. den
المساهمون: Ophthalmology
المصدر: American Journal of Human Genetics, 93, 110-7
The American Journal of Human Genetics; Vol 93
American Journal of Human Genetics, 93, 1, pp. 110-7
American Journal of Human Genetics, 93(1), 110-117. Cell Pressمصطلحات موضوعية: Genetics and epigenetic pathways of disease [NCMLS 6], genetic structures, Visual Acuity, GTPase, Retinal Pigment Epithelium, Retinal Rod Photoreceptor Cells, Evaluation of complex medical interventions Genomic disorders and inherited multi-system disorders [NCEBP 2], Genetics(clinical), Child, Genetics (clinical), Genetics, 0303 health sciences, 030305 genetics & heredity, Homozygote, Chromosome Mapping, Disease gene identification, Pedigree, Isoenzymes, Protein Transport, medicine.anatomical_structure, Codon, Nonsense, Retinitis Pigmentosa, Adult, Adolescent, Nonsense mutation, Protein Prenylation, Genes, Recessive, Biology, Retina, Genomic disorders and inherited multi-system disorders [IGMD 3], 03 medical and health sciences, Report, Retinitis pigmentosa, Ciliary rootlet, medicine, Animals, Humans, Genetic Predisposition to Disease, Cilia, Photoreceptor Connecting Cilium, Genetic Association Studies, 030304 developmental biology, Retinal pigment epithelium, Genetics and epigenetic pathways of disease Plasticity and memory [NCMLS 6], medicine.disease, Molecular biology, eye diseases, Rats, Alternative Splicing, Gene Expression Regulation, rab GTP-Binding Proteins, Protein prenylation, Rab, sense organs, Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6]
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcbdd8c3d9e814ec7ff86694f085cc8cTest
https://hdl.handle.net/1765/54752Test -
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المؤلفون: Neveling, K., Hollander, A.I. den, Cremers, F.P.M., Collin, R.W.J.
المصدر: Methods in Molecular Biology, 935, 3-23
Methods in Molecular Biology, 935, pp. 3-23مصطلحات موضوعية: Genomic disorders and inherited multi-system disorders [IGMD 3], Genetics and epigenetic pathways of disease [NCMLS 6], Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6]
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::aaf81a281057dcf6eb27d945458a132eTest
https://hdl.handle.net/2066/118575Test -
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المؤلفون: Stefanie Märzheuser, Heiko Reutter, Franziska Degenhardt, Markus M. Nöthen, Tracie Pennimpede, Hartmut Engels, Lars Wittler, Michael Ludwig, Gabriel C. Dworschak, Markus Draaken, Friedhelm Hildebrandt, Sabine Grasshoff-Derr, Iris A.L.M. van Rooij, Enrika Bartels, Carlo Marcelis, Charlotte Schramm, Eberhard Schmiedeke, Charlotte H. W. Wijers, Alina C. Hilger, Alexander M. Zink, Stuart Hosie, Bernhard G. Herrmann, Stefan Holland-Cunz, Annette M. Müller
المصدر: European journal of human genetics : EJHG ; the official journal of the European Society of Human Genetics
European Journal of Human Genetics, 21, 12, pp. 1377-82
European Journal of Human Genetics, 21, 1377-82مصطلحات موضوعية: Heart Defects, Congenital, Male, medicine.medical_specialty, Candidate gene, DNA Copy Number Variations, Limb Deformities, Congenital, Anal Canal, Tracheoesophageal fistula, Biology, Kidney, Gastroenterology, digestive system, Article, Receptors, G-Protein-Coupled, Anus, Imperforate, Genomic disorders and inherited multi-system disorders [IGMD 3], Mice, Esophagus, Internal medicine, Genetics, medicine, Animals, Humans, Abnormalities, Multiple, Copy-number variation, Genetics (clinical), Human Reproducion Genomic disorders and inherited multi-system disorders [NCEBP 12], medicine.disease, VACTERL association, Phenotype, Spine, digestive system diseases, Trachea, Radius, medicine.anatomical_structure, Human Reproduction Renal disorder [NCEBP 12], Atresia, Karyotyping, Female, SNP array
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae3804f14a988999d6146fe14e3be0efTest
https://hdl.handle.net/2066/125305Test