-
1
المؤلفون: A Vandenberghe, H Heylen, G. Mertens, L Boutrand, Z.N Berneman, N Mommers
المصدر: International Congress Series. 1239:943-946
مصطلحات موضوعية: Genetics, Mutation rate, education.field_of_study, First line, Population, General Medicine, Biology, humanities, symbols.namesake, Mendelian inheritance, symbols, Microsatellite, Multiplex, Typing, Restriction fragment length polymorphism, education
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::a62e85257c5852c12418c3773afe88aeTest
https://doi.org/10.1016/s0531-5131Test(02)00560-5 -
2
المؤلفون: G. Mertens, N Mommers, A Vandenberghe, M. Gielis, L Boutrand
المصدر: International Journal of Legal Medicine. 115:40-44
مصطلحات موضوعية: Mutation rate, Population, Population genetics, Locus (genetics), Biology, Pathology and Forensic Medicine, Belgium, Humans, Allele, education, Allele frequency, Alleles, DNA Primers, Genetics, education.field_of_study, Polymorphism, Genetic, Base Sequence, Forensic Medicine, DNA Fingerprinting, humanities, language.human_language, Flemish, Genetics, Population, DNA profiling, Tandem Repeat Sequences, Mutation, language
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce60d1b8e95bf07ca3f3c2f7372a3f7dTest
https://doi.org/10.1007/s004140100227Test -
3
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 -
4
المؤلفون: S. Füredi, Balázs Egyed, G. Mertens, N Mommers, A Vandenberghe, L Boutrand
المصدر: International journal of legal medicine. 114(4-5)
مصطلحات موضوعية: Genetics, Polymorphism, Genetic, Locus (genetics), Paternity, Biology, DNA Fingerprinting, humanities, Pathology and Forensic Medicine, Molecular level, Tandem Repeat Sequences, Drop out, CD4 Antigens, Str loci, Microsatellite, Humans, Typing, Primer (molecular biology), Allele, Diagnostic Errors, Alleles, DNA Primers
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::337d86a10c347660bd5680c7717f42b3Test
https://pubmed.ncbi.nlm.nih.gov/11355416Test -
5
المؤلفون: N, Bissar-Tadmouri, Y, Parman, L, Boutrand, F, Deymeer, P, Serdaroglu, A, Vandenberghe, E, Battaloglu
المصدر: Clinical genetics. 58(5)
مصطلحات موضوعية: Adult, Male, Polymorphism, Genetic, Adolescent, Genotype, Turkey, DNA Mutational Analysis, Peripheral Nervous System Diseases, Connexins, Phenotype, Charcot-Marie-Tooth Disease, Humans, Female, Child, Myelin Proteins
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::0f38807e2bb9edfd877e658b83ad7977Test
https://pubmed.ncbi.nlm.nih.gov/11140841Test -
6
المؤلفون: Zs Pádár, A Vandenberghe, M. Angyal, L Boutrand, J. Woller, S. Füredi, Balázs Egyed
المصدر: Forensic science international. 113(1-3)
مصطلحات موضوعية: Electrophoresis, Male, Mutation rate, Roma, Genotype, Databases, Factual, Population, Yugoslavia, Population genetics, Locus (genetics), Paternity, Minisatellite Repeats, Biology, Polymerase Chain Reaction, Sampling Studies, White People, Pathology and Forensic Medicine, Consanguinity, Gene Frequency, Population Database, Humans, Allele, education, Allele frequency, Genetics, education.field_of_study, Hungary, Polymorphism, Genetic, Genetic Variation, Forensic Medicine, DNA Fingerprinting, humanities, Genetics, Population, Tandem Repeat Sequences, Data Interpretation, Statistical, Albania, Mutation, Str loci, Microsatellite, Female, Law, Software
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e8e38941baa41ebbb0bc2f2f55e0560Test
https://pubmed.ncbi.nlm.nih.gov/10978596Test -
7
المؤلفون: L. Boutrand, P. Petiot, G. Chamba, R. Besançon, A. Vandenberghe, Philippe Latour, L. Konecny, A.L. Prost, N. Kopp, A. Mularoni
المصدر: FEBS letters. 457(3)
مصطلحات موضوعية: Adult, Male, Transcription, Genetic, Biophysics, Exonic splicing enhancer, Biology, Splicing, Biochemistry, Polymerase Chain Reaction, Exon, Myelin, Major protein zero, Structural Biology, Transcription (biology), Charcot-Marie-Tooth Disease, Peripheral Nervous System, Genetics, medicine, Leukocytes, Humans, Molecular Biology, Gene, DNA Primers, Polymorphism, Genetic, Alternative splicing, RNA, Premature termination codon, Cell Biology, Exons, Middle Aged, Molecular biology, Actins, Alternative Splicing, medicine.anatomical_structure, Organ Specificity, RNA splicing, Codon, Terminator, Myelin P0 Protein
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbdecb2da40df59e00ee6625e9ac2e87Test
https://pubmed.ncbi.nlm.nih.gov/10471804Test -
8
المؤلفون: O M, Sinilnikova, K M, Egan, J L, Quinn, L, Boutrand, G M, Lenoir, D, Stoppa-Lyonnet, L, Desjardins, C, Levy, D, Goldgar, E S, Gragoudas
المصدر: International journal of cancer. 82(3)
مصطلحات موضوعية: Male, Eye Neoplasms, Humans, Female, Genetic Predisposition to Disease, Genetic Testing, Middle Aged, Melanoma, Germ-Line Mutation, Neoplasm Proteins
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::2ae1923f78e856ad7cfbc8ef2b2cb0faTest
https://pubmed.ncbi.nlm.nih.gov/10399947Test -
9
المؤلفون: O M, Serova-Sinilnikova, L, Boutrand, D, Stoppa-Lyonnet, B, Bressac-de-Paillerets, V, Dubois, C, Lasset, N, Janin, Y J, Bignon, M, Longy, C, Maugard, R, Lidereau, D, Leroux, T, Frebourg, S, Mazoyer, G M, Lenoir
المصدر: American journal of human genetics. 60(5)
مصطلحات موضوعية: Adult, BRCA2 Protein, Male, Ovarian Neoplasms, Letter, Mutation, Humans, Breast Neoplasms, Female, France, Middle Aged, Neoplasm Proteins, Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::512dc4fb8917648d7898fd9c5d55e696Test
https://pubmed.ncbi.nlm.nih.gov/9150172Test -
10
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