-
1
المؤلفون: Francesco Palau, Merle Ruberg, Kaisa Silander, Antoon Vandenberghe, S. Tardieu, Ian P. Blair, Alexis Brice, Judith Lopes, Eric LeGuern
المصدر: Publons
مصطلحات موضوعية: Heterozygote, congenital, hereditary, and neonatal diseases and abnormalities, DNA Repair, DNA damage, DNA repair, Saccharomyces cerevisiae, Biology, chemistry.chemical_compound, Charcot-Marie-Tooth Disease, Genetics, Humans, Gene conversion, Molecular Biology, Genetics (clinical), Recombination, Genetic, Models, Genetic, DNA, General Medicine, Gene rearrangement, Double Strand Break Repair, chemistry, DNA mismatch repair, Hereditary Sensory and Motor Neuropathy, Chromosomes, Human, Pair 17, DNA Damage, Heteroduplex
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8303a7f782f896cd2719e86d2dc2d34Test
https://doi.org/10.1093/hmg/8.12.2285Test -
2
المؤلفون: Antoon Vandenberghe, Alain Lachaux, Michèle Accominotti, Muriel Bost
المصدر: The Journal of Trace Elements in Experimental Medicine. 12:321-329
مصطلحات موضوعية: Genetics, Haplotype, Locus (genetics), Single-strand conformation polymorphism, Biology, Chronic liver disease, medicine.disease, Biochemistry, Molecular biology, Exon, medicine, Polymorphic Microsatellite Marker, Missense mutation, Gene
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::dbea9b145fe06a82288d44a923ccb6a2Test
https://doi.org/10.1002Test/(sici)1520-670x(1999)12:4<321::aid-jtra5>3.0.co;2-y -
3
المؤلفون: Merle Ruberg, Alexis Brice, N. Ravisé, Victor Ionasescu, Michelle Mayer, Nobutada Tachi, Philippe Latour, Antoon Vandenberghe, Francisco Palau, Nicholas W. Wood, Pierre Bouche, Judith Lopes, Eric LeGuern, Nicolas Lévy
المصدر: Human Molecular Genetics. 7:141-148
مصطلحات موضوعية: Genetics, Breakpoint, General Medicine, Gene rearrangement, Biology, Chromosome 17 (human), Meiosis, Gene mapping, Gene duplication, Homologous recombination, Molecular Biology, Gene, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::b45cccff9890b350e6ddc476abaf17e0Test
https://doi.org/10.1093/hmg/7.1.141Test -
4
المؤلفون: Nathalie Roeckel, Blanquet F, André Dautigny, Marie Geneviève Mattei, Philippe Latour, Guy Chazot, Danielle Pham-Dinh, Antoon Vandenberghe, Fourbil Y
المصدر: Human Molecular Genetics. 2:2051-2054
مصطلحات موضوعية: Yeast artificial chromosome, congenital, hereditary, and neonatal diseases and abnormalities, Genetic Linkage, Cell Adhesion Molecules, Neuronal, Molecular Sequence Data, Restriction Mapping, Biology, Polymerase Chain Reaction, Myelin, Gene mapping, Charcot-Marie-Tooth Disease, Gene cluster, Leukocytes, Genetics, medicine, Humans, Amino Acid Sequence, Receptor, Chromosomes, Artificial, Yeast, Molecular Biology, Gene, Genetics (clinical), DNA Primers, Polymorphism, Genetic, Base Sequence, Genes, Immunoglobulin, Receptors, IgG, Nucleic acid sequence, Chromosome Mapping, Chromosome, Exons, General Medicine, medicine.anatomical_structure, Chromosomes, Human, Pair 1, Immunoglobulin G, Multigene Family, Myelin P0 Protein, Myelin Proteins, Demyelinating Diseases
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::580850ffeeaf36639f3e3c0f999dfb92Test
https://doi.org/10.1093/hmg/2.12.2051Test -
5
المؤلفون: Philippe Latour, P Diraison, Antoon Vandenberghe, Christine Bonnebouche, Michel Boucherat, Muriel Bost, Françoise Chapon
المصدر: Clinical Genetics. 46:327-328
مصطلحات موضوعية: Male, Genetics, Myelin protein zero, Locus (genetics), Biology, Myelin P0 Protein, Molecular biology, Pedigree, Charcot-Marie-Tooth Disease, Chromosomes, Human, Pair 1, Humans, Restriction fragment length polymorphism, Deoxyribonucleases, Type II Site-Specific, Myelin Proteins, Polymorphism, Restriction Fragment Length, Genetics (clinical), Genes, Dominant
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae740794fe8dba1f7e04d4982f6a486eTest
https://doi.org/10.1111/j.1399-0004.1994.tb04172.xTest -
6
المؤلفون: Antoon Vandenberghe, Eva Nelis, André Dautigny, Christine Van Broeckhoven, Jean-Jacques Martin, Peter De Jonghe, Vincent Timmerman, Danielle Pham-Dinh
المصدر: Human genetics
مصطلحات موضوعية: Silent mutation, Genetics, Polymorphism, Genetic, Base Sequence, Myelin protein zero, Nonsense mutation, Molecular Sequence Data, Biology, Molecular biology, Exon, Charcot-Marie-Tooth Disease, Peripheral myelin protein 22, Gene duplication, Mutation, Missense mutation, Humans, Human medicine, Gene, Myelin P0 Protein, Genetics (clinical), Myelin Proteins, Polymorphism, Single-Stranded Conformational
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77fbbc8991b147fbb2cd9e5c697b6b7aTest
https://pubmed.ncbi.nlm.nih.gov/7527371Test -
7
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 -
8
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 -
9
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 -
10
المؤلفون: M. Hamel, B. Lechevalier, Antoon Vandenberghe, Ph. Diraison, S. Schaeffer, Ph. Latour, Françoise Chapon
المصدر: Neuromuscular Disorders. 7:472
مصطلحات موضوعية: Electrophysiology, Neurology, Pediatrics, Perinatology and Child Health, Neurology (clinical), Biology, Gene, Molecular biology, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::569211fb031e289e64f012ae0b9cd8f7Test
https://doi.org/10.1016/s0960-8966Test(97)87343-9