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المؤلفون: Wim Van Hul, A. Wehnert, Guy Van Camp, Antoon Vandenberghe, H Backhovens, David Patterson, Piet Stinissen, Christine Van Broeckhoven
المصدر: Somatic cell and molecular genetics. 16(3)
مصطلحات موضوعية: Genetic Markers, Chromosomes, Human, Pair 21, Centromere, Locus (genetics), Biology, Hybrid Cells, Mice, Alzheimer Disease, Chromosome regions, Genetics, medicine, Animals, Humans, Bacteriophages, Cloning, Molecular, Chromosome Mapping, Cell Biology, General Medicine, medicine.disease, Molecular biology, Somatic fusion, Blotting, Southern, Genetic marker, Trisomy, Chromosome 21, DNA Probes, Chromosome 22, Polymorphism, Restriction Fragment Length
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d67f7ea44f7bf4c3df21a7627621156cTest
https://pubmed.ncbi.nlm.nih.gov/1972817Test -
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المصدر: Nucleic acids research
مصطلحات موضوعية: Genetics, Male, biology, Chromosomes, Human, Pair 21, EcoRI, Locus (genetics), Deoxyribonuclease EcoRI, Molecular biology, Pedigree, Chemistry, Gene mapping, biology.protein, Humans, Female, Restriction fragment length polymorphism, Molecular probe, Allele frequency, Biology, Polymorphism, Restriction Fragment Length
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f18153fed9bd5f21c97ba937876d4bbbTest
https://pubmed.ncbi.nlm.nih.gov/1969629Test -
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المؤلفون: Ronald J. Polinsky, B. O'Donnell, Leonard L. Heston, A. Haynes, L. Bergamini, G. De Winter, H Backhovens, J. F. Foncin, L. Connor, C. Van Broeckhoven, Richard H. Myers, David A. Drachman, Stefano F. Cappa, K. Abe, Luigi Amaducci, John Hardy, J. J. Martin, Lindsay A. Farrer, Antoon Vandenberghe, H. Karlinsky, Richard Mayeux, L. Pinessi, C. Ruiz, M. E. Percy, Rossella Tupler, J. Henry, D. R. Crapper McLachlan, Robert G. Feldman, Martin N. Rossor, M.P. Montesi, Daniel A. Pollen, P. Frommelt, M. Mortilla, P Roques, James F. Gusella, M. Fracarro, Jonathan L. Haines, Voskresenskaya Ni, L James, Michael Mullan, Paul C. Watkins, V. A. Fried, Linda Nee, P. St. George-Hyslop, J. M. Cantu, Amalia C. Bruni, N. Nacmias, Sandro Sorbi, G. Vaula, Robert Williamson, Innocenzo Rainero, Alison Goate, Gavrilova Si, John H. Growdon, M. Vartanian, M. J. Owen, G. Gei, Marianne James, Stephen S. Rich, Rudolph E. Tanzi, J. Swearer, Marc Bruyland, Harry T. Orr, M. E. Franco, Silvia Piacentini, J. Gheuens
المصدر: Nature
مصطلحات موضوعية: Genetic Markers, Genetics, Heterozygote, Multidisciplinary, Chromosomes, Human, Pair 21, Genetic Linkage, Genetic heterogeneity, Pedigree chart, Disease, Biology, medicine.disease, Pedigree, Gene mapping, Alzheimer Disease, Genetic marker, Genetic linkage, medicine, Humans, Lod Score, Alzheimer's disease, Chromosome 21, Engineering sciences. Technology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c81e757dca0d17ac30011aa71a54324Test
https://hdl.handle.net/10067/1434090151162165141Test -
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المؤلفون: Antoon Vandenberghe, A. Wehnert, J. J. Martin, W. Van Hul, G. Van Camp, C. Van Broeckhoven, H Backhovens, G. De Winter, J. Gheuens, Piet Stinissen, Marc Bruyland, P Raeymaekers
المصدر: Neuropsychopharmacology ISBN: 9783642740367
Neuropsychopharmacology / Bunney, W.E. [edit.]مصطلحات موضوعية: business.industry, Hippocampus, Pedigree chart, Autopsy, Disease, medicine.anatomical_structure, Cerebral cortex, Genetic marker, Immunology, Medicine, Human medicine, Senile plaques, Family history, business, Biology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2726cac7c4884c90f5c4cffe54fbee0fTest
https://doi.org/10.1007/978-3-642-74034-3_9Test -
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المؤلفون: Françoise Chapon, Antoon Vandenberghe, Philippe Latour, Christine Bonnebouche, P Diraison, Françoise Blanquet-Grossard, André Dautigny, Danielle Pham-Dinh, Guy Chazot
المصدر: Human Mutation. 8:185-186
مصطلحات موضوعية: chemistry.chemical_classification, chemistry.chemical_compound, Glycosylation, chemistry, Peripheral myelin, Mutation (genetic algorithm), Genetics, Biology, Glycoprotein, Molecular biology, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::000d73af3151426450e94a5cffa67d15Test
https://doi.org/10.1002Test/(sici)1098-1004(1996)8:2<185::aid-humu13>3.0.co;2-z -
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المؤلفون: N Vandenberghe, Guy Chazot, A Gatignol, M Boucherat, M Upadhyaya, L. Boutrand, Antoon Vandenberghe, Philippe Latour
المصدر: Journal of Medical Genetics. 39:81e-81
مصطلحات موضوعية: Male, Early Growth Response Protein 2, DNA Mutational Analysis, Schwann cell, Myelin, Gene Frequency, Charcot-Marie-Tooth Disease, Peripheral myelin protein 22, Genetics, medicine, Humans, Genetic Testing, education, Polymorphism, Single-Stranded Conformational, Genetics (clinical), Zinc finger, education.field_of_study, biology, Myelin protein zero, Zinc Fingers, Myelin basic protein, DNA-Binding Proteins, Hereditary Central Nervous System Demyelinating Diseases, Phenotype, medicine.anatomical_structure, Mutation, biology.protein, Connexin 32, Female, Online Mutation Report, Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::065da6edfad46a37cd94ae26179126c1Test
https://doi.org/10.1136/jmg.39.12.e81Test -
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المؤلفون: Antoon Vandenberghe, Konecny Lara, Philippe Latour, Boutrand Laetitia, Roger Besançon, Geneviève Chamba, Angélique Mularoni
المصدر: Human Mutation. 17:237-237
مصطلحات موضوعية: Genetics, business.industry, Single-nucleotide polymorphism, PMP2, Biology, medicine.disease, Peripheral myelin protein, Peripheral neuropathy, Text mining, medicine, SNP, business, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::b025036a1aa4ddf7caa881435276c5daTest
https://doi.org/10.1002/humu.11Test -
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المؤلفون: Feza Deymeer, Nisrine Bissar-Tadmouri, Yesim Gulsen-Parman, Piraye Serdaroglu, Esra Battaloglu, Antoon Vandenberghe, Philippe Latour
المصدر: Human Mutation. 14:449-449
مصطلحات موضوعية: Adult, Male, Turkey, Turkish, Molecular Sequence Data, Mutation, Missense, Biology, Type (biology), Charcot-Marie-Tooth Disease, Genetics, Humans, Point Mutation, Coding region, Amino Acid Sequence, Gene, Polymorphism, Single-Stranded Conformational, Genetics (clinical), Base Sequence, Myelin protein zero, Sequence Analysis, DNA, Middle Aged, language.human_language, Mutagenesis, Insertional, Amino Acid Substitution, Chromosomes, Human, Pair 1, language, Female, Chromosome Deletion, Myelin P0 Protein
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cb128b405745999000445f2d279c49aTest
https://doi.org/10.1002Test/(sici)1098-1004(199911)14:5<449::aid-humu17>3.0.co;2-h -
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المؤلفون: Alberta Lorenzi, Franck Sturtz, Antoon Vandenberghe, Roger Besançon, Christine Van Broeckhoven, Emmanuel Broussolle, Guy Chazot, Geneviève Chamba, Sandrine Radawiec, Marc Cruts
المصدر: Human Mutation. 11:481-481
مصطلحات موضوعية: Genetics, Exon, Transmission (medicine), medicine, Missense mutation, Early-onset Alzheimer's disease, Biology, medicine.disease, Genetics (clinical), Presenilin 1 Gene, Allele specific
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::6e3cc1b9c5c4d4d30e9799eaa38a8cb1Test
https://doi.org/10.1002Test/(sici)1098-1004(1998)11:6<481::aid-humu13>3.0.co;2-n -
50
المؤلفون: Antoon Vandenberghe, Philippe Latour, A Brice, E. Le Guern, N. Ravisé, Judith Lopes, Victor Ionasescu, S. Tardieu
المصدر: Neuromuscular Disorders. 7:471
مصطلحات موضوعية: Genetics, Neurology, Pediatrics, Perinatology and Child Health, Crossover, Breakpoint, Neurology (clinical), Biology, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::9dc7ce1f50a2a463586983652c553805Test
https://doi.org/10.1016/s0960-8966Test(97)87340-3