-
1
المؤلفون: J. Gheuens, J. J. Martin, Michael Mullan, Gerd Multhaup, N.G. Irving, Antoon Vandenberghe, Hugh Gurling, W. Van Hul, A. Genthe, John Hardy, A. Wehnert, A. Barton, M. Salbaum, Bernhard Horsthemke, Marc Bruyland, H Backhovens, S. J. Richards, Konrad Beyreuther, C. Van Broeckhoven, A. Holland, Robert Williamson, Colin L. Masters, Peter Raeymaekers, Patrick Cras
المصدر: Nature
مصطلحات موضوعية: Adult, Male, Amyloid, Chromosomes, Human, Pair 21, Genetic Linkage, Locus (genetics), Disease, Biology, Alzheimer Disease, Genetic linkage, medicine, Humans, Senile plaques, Protein Precursors, Genetics, Amyloid beta-Peptides, Polymorphism, Genetic, Multidisciplinary, Molecular pathology, Chromosome Mapping, medicine.disease, Pedigree, Genes, Female, Alzheimer's disease, Chromosome 21, Engineering sciences. Technology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f73777dee0f802153a1b26c3c1a5967aTest
https://doi.org/10.1038/329153a0Test -
2
المؤلفون: Nisrine Bissar-Tadmouri, Piraye Serdaroglu, Yesim Parman, L Boutrand, Feza Deymeer, Antoon Vandenberghe, Esra Battaloglu
المصدر: Clinical Genetics. 58:396-402
مصطلحات موضوعية: Genetics, education.field_of_study, Myelin protein zero, Point mutation, Locus (genetics), Biology, Frameshift mutation, Genotype, Gene duplication, Connexin 32, education, Gene, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::cdea0c3e5853b6b95298dd650606b876Test
https://doi.org/10.1034/j.1399-0004.2000.580511.xTest -
3
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
-
4
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 -
5
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 -
6
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 -
7
المؤلفون: C. Van Broeckhoven, Antoon Vandenberghe, G. Van Camp
المصدر: Human genetics
مصطلحات موضوعية: Genetics, Chromosomes, Human, Pair 21, Hybridization probe, Locus (genetics), Biology, Cosmids, Human genetics, Deoxyribonuclease HpaII, Blotting, Southern, Gene mapping, Gene Frequency, Alzheimer Disease, Cosmid, Humans, Human medicine, Restriction fragment length polymorphism, Allele, DNA Probes, Deoxyribonucleases, Type II Site-Specific, Allele frequency, Genetics (clinical), Alleles, Polymorphism, Restriction Fragment Length
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::561e52fc94388ce1cae22d07625f74a9Test
https://pubmed.ncbi.nlm.nih.gov/1694162Test -
8
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 -
9
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 -
10
المصدر: Nucleic acids research
مصطلحات موضوعية: Genetics, Base Sequence, Chromosomes, Human, Pair 21, Inverse polymerase chain reaction, Molecular Sequence Data, Locus (genetics), Biology, Polymerase Chain Reaction, Molecular biology, law.invention, Terminal restriction fragment length polymorphism, law, Cleaved amplified polymorphic sequence, Humans, Amplified fragment length polymorphism, Human medicine, Restriction fragment length polymorphism, Simple sequence length polymorphism, Polymorphism, Restriction Fragment Length, Polymerase chain reaction
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::595d257cf526bedf06d1b63d3b721af2Test
https://doi.org/10.1093/nar/18.12.3672Test