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1
المؤلفون: Philippe Latour, Antoon Vandenberghe, André Dautigny, Emmanuel Corbillon, Jacques Battin, Catherine Ressot, Elizabeth Ollagnon, Françoise Serville, Franck Sturtz, Sylvie Duthel, Danielle Pham-Dinh, Françoise Blanquet-Grossard
المصدر: Human genetics. 98(2)
مصطلحات موضوعية: Male, X Chromosome, Genetic Linkage, Nonsense mutation, Biology, medicine.disease_cause, Diagnostic tools, Polymerase Chain Reaction, Connexins, Charcot-Marie-Tooth Disease, Genetics, medicine, Missense mutation, Coding region, Humans, Point Mutation, Amino Acid Sequence, Codon, Gene, Genetics (clinical), Polymorphism, Single-Stranded Conformational, Genes, Dominant, Mutation, Base Sequence, DNA, Human genetics, Pedigree, Codon, Nonsense, Female, X-linked dominant
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59acb3d7f6ed0dd25dc93ed4a2594848Test
https://pubmed.ncbi.nlm.nih.gov/8698335Test -
2
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 -
3
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 -
4
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 -
5
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