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1
المؤلفون: Ahmed Bouhouche, Mohamed Yahyaoui, T. Chkili, Antoon Vandenberghe, Nazha Birouk, Angélique Mularoni, Djamal Grid, Johann Tassin, Ali Benomar, Alexis Brice, Eric LeGuern, Farid Meggouh
المساهمون: Other departments
المصدر: American journal of human genetics, 65(3), 722-727. Cell Press
مصطلحات موضوعية: Adult, Genetic Markers, Male, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, Locus (genetics), Genes, Recessive, Genetic mapping, Consanguinity, Biology, Charcot-Marie-Tooth disease, P0 gene, Genetic determinism, Gene mapping, Autosomal recessive form, Genetics, Humans, Genetics(clinical), Age of Onset, Child, Chromosomes, Artificial, Yeast, Genetics (clinical), Recombination, Genetic, Haplotype, Homozygote, Axonal form, Chromosome, Chromosome Mapping, Middle Aged, Axons, Pedigree, Morocco, Haplotypes, Genetic marker, Chromosomes, Human, Pair 1, Chromosome 1q21.2-q21.3, Female, Age of onset, Lod Score, Myelin P0 Protein, Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28df11cb04624edf0cbea80cff137fbaTest
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2
المؤلفون: J.J. Martin, John Hardy, Alison Goate, Martin N. Rossor, C. Van Broeckhoven, A. Hofman, Antoon Vandenberghe, C M van Duijn, Michael Mullan
المصدر: The British journal of psychiatry
Scopus-Elsevierمصطلحات موضوعية: Genetic Markers, Chromosomes, Human, Pair 21, Genetic Linkage, Genetic counseling, Population, Chromosome Disorders, Locus (genetics), Biology, 03 medical and health sciences, 0302 clinical medicine, Alzheimer Disease, Risk Factors, Genetic linkage, medicine, Humans, Early-onset Alzheimer's disease, 030212 general & internal medicine, Allele, education, Alleles, Aged, Genes, Dominant, Chromosome Aberrations, Genetics, education.field_of_study, Models, Genetic, Genetic Carrier Screening, Middle Aged, medicine.disease, 030227 psychiatry, Psychiatry and Mental health, Allelic heterogeneity, Age of onset
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c70ad08011c348c79b3f8050ef157e93Test
https://doi.org/10.1192/bjp.158.4.471Test -
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المؤلفون: Nicole Philip, Philippe Latour, Perrine Malzac, Amandine Boyer, P. Negre, Rafaëlle Bernard, Antoon Vandenberghe, Nicolas Lévy
المصدر: European journal of human genetics : EJHG. 10(5)
مصطلحات موضوعية: Genetic Markers, Male, Pediatrics, medicine.medical_specialty, Genetic counseling, Prenatal diagnosis, Disease, Genetic Heterogeneity, Charcot-Marie-Tooth Disease, Pregnancy, Prenatal Diagnosis, Gene duplication, Genetics, medicine, Humans, Genetics (clinical), Fetus, business.industry, Genetic heterogeneity, medicine.disease, Charcot-Marie-Tooth Disease Type 1A, Pedigree, Fetal Diseases, Female, business, Gene Deletion, Chromosomes, Human, Pair 17
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a586e28087ad8108865355fad3fe17fcTest
https://pubmed.ncbi.nlm.nih.gov/12082504Test -
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المؤلفون: Pierre Cochat, Claude Dupont, Christine Bonnebouche, Antoon Vandenberghe, Pierre-Marie Gonnaud, Guy Chazot, Muriel Bost, Brigitte Gilbert
المصدر: Clinical genetics. 46(5)
مصطلحات موضوعية: Genetics, Genetic Markers, Male, Biology, medicine.disease, Pedigree, Central nervous system disease, Degenerative disease, Gene Frequency, Genetic marker, Charcot-Marie-Tooth Disease, Multigene Family, Gene duplication, medicine, Humans, Female, Allele, Molecular probe, DNA Probes, Genetics (clinical), Alleles, Chromosomes, Human, Pair 17
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03d2e9d81a51fb610e4c25c2f74c85a2Test
https://pubmed.ncbi.nlm.nih.gov/7889651Test -
5
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 -
6
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: Anita Wehnert, Peter Raeymaekers, Peter De Jonghe, Christine Van Broeckhoven, Jean-Jacques Martin, Antoon Vandenberghe, Jan Ghenens, Hubert Backhovens, Ludo Muylle
المصدر: Human Genetics. 81:231-233
مصطلحات موضوعية: Genetic Markers, Genetics, Genetic Linkage, Karyotype, Locus (genetics), Biology, Complete linkage, Chromosome Banding, Muscular Atrophy, Spinal, Gene mapping, Charcot-Marie-Tooth Disease, Chromosomes, Human, Pair 1, Genetic linkage, Genetic marker, Blood Group Antigens, Humans, Duffy Blood-Group System, Gene, Genetics (clinical), Sex linkage
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89234c93a42d5de904b56ad54a801d31Test
https://doi.org/10.1007/bf00278994Test -
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المؤلفون: Antoon Vandenberghe, Peter Raeymaekers, Ludo Muylle, H Backhovens, Christine Van Broeckhoven, A. Wehnert, Peter De Jonghe, J. Gheuens
المصدر: Human genetics
مصطلحات موضوعية: Genetic Markers, Male, Genetic Linkage, Locus (genetics), Biology, Muscular Atrophy, Spinal, Tooth disease, Charcot-Marie-Tooth Disease, Genetics, Humans, Spectrin, Metabolic disease, Genetics (clinical), α spectrin, Genes, Dominant, Lod score, Chromosome Mapping, Human genetics, Pedigree, Blood Group Antigens, Female, Human medicine, Restriction fragment length polymorphism, Duffy Blood-Group System, Polymorphism, Restriction Fragment Length
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::818c89e230018f711920ea20ffcb199aTest
https://hdl.handle.net/10067/1002070151162165141Test -
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المؤلفون: A. Wehnert, Antoon Vandenberghe, J. Gheuens, J. J. Martin, C. Van Broeckhoven, P. De Jonghe, H Backhovens, G. De Winter, L. Swerts, P Raeymaekers
المصدر: Neurology
مصطلحات موضوعية: Genetics, Genetic Markers, Polymorphism, Genetic, Genetic heterogeneity, Genetic Linkage, Locus (genetics), Disease, DNA, Biology, medicine.disease, Muscular Atrophy, Spinal, Tooth disease, Degenerative disease, Genetic linkage, Genetic marker, Charcot-Marie-Tooth Disease, Chromosomes, Human, Pair 1, medicine, Humans, Neurology (clinical), Human medicine, Gene, Software
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aee6fcf579b0af404067ba18671d609fTest
https://pubmed.ncbi.nlm.nih.gov/2725880Test