9th International workshop on Fragile X syndrome and X‐linked mental retardation

Identifieur interne : 00C032 ( Main/Exploration ); précédent : 00C031; suivant : 00C033

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9th International workshop on Fragile X syndrome and X‐linked mental retardation

Auteurs : Jean-Pierre Fryns [Belgique] ; Martine Borghgraef [Belgique] ; Ted W. Brown [États-Unis] ; Jamel Chelly [France] ; Gene S. Fisch [États-Unis] ; Ben Hamel [Pays-Bas] ; André Hanauer [France] ; Didier Lacombe [France] ; Ligun Luo [États-Unis] ; James N. Macpherson [Royaume-Uni] ; Jean-Louis Mandel [France] ; Claude Moraine [France] ; John Mulley [Australie] ; David Nelson [États-Unis] ; Ben Oostra [Pays-Bas] ; Michael Partington [Australie] ; Ger J. A. Ramakers [Pays-Bas] ; Hans-Hilger Ropers [Allemagne] ; François Rousseau [Canada] ; Charles Schwartz [États-Unis] ; Peter Steinbach [Allemagne] ; Claude Stoll [France] ; Lisbeth Tranebjaerg [Norvège] ; Gillian Turner [Australie] ; Hans Van Bokhoven [Pays-Bas] ; Angela Vianna-Morgante [Brésil] ; Laurent Villard [France] ; Stephen T. Warren [Géorgie (pays)]

Source :

• American Journal of Medical Genetics [ 0148-7299 ] ; 2000-10-23.

RBID : ISTEX:4659AC135A9DD1BEB7353D4F2A9EB67D3C75FEF2

Descripteurs français

• Wicri :
  • geographic : Belgique, Pays-Bas.
  • topic : Recherche fondamentale, Génétique, Recherche médicale.

English descriptors

• KwdEn :
  • Academic university, Actin cytoskeleton, Actin cytoskeleton organization, Adaptive behavior, Allele, Andre hanauer, Andrea peier, Andrea sharrock, Angela viannamorgante, Balanced translocation, Barbara bardoni, Basic research, Baylor college, Baylor plaza, Belgium, Biological sciences, Bipolar affective disorder, Brain research, Candidate genes, Carola bontekoe, Caroline moore, Cdna, Cdna microarrays, Cedex, Cell lines, Cellular mechanisms, Centre hosp, Charles schwartz, Chelly, Child development unit, Claude moraine, Claude stoll, Claudia bagni, Clinical genetics, Clinical genetics department, Clinical genetics dept, Clinical referrals, Cognitive impairment, Conference report, Corresponding genes, Dana crawford, Daniela toniolo, David nelson, Deletion, Dendritic, Dept, Developmental disabilities, Didier lacombe, Diego otero, Different populations, Elizabeth hinkle, Emory university, Erasmus, Erasmus university, Erasmus university rotterdam, European xlmr consortium, Flora tassone, Fmr1, Fmr1 alleles, Fmr1 gene, Fmr1 gene expression, Fmr1 knockout mice, Fmr1 mrna, Fmr1 mrna expression, Fmr1 mutation, Fmr1 triplets, Fmr2, Fmr2 gene, Fmr2 mutation, Fmrp, Forest hill road, Fragile, Francois rousseau, Frank kooy, Fraxa, Fraxe, Fryns, Full mutation, Full mutation alleles, Fullmutation alleles, Gene, Genet, Genetic background, Genetica, Genetica medica, Genetics, Genetics laboratory, Genetique medicale, Germ cells, Gillian turner, Greenwood, Gregor mendel circle, Hamel, Helger yntema, Herestraat, Histone deacetylases, Hopital saint antoine, Hospital clinic, Human genetics, Hunter genetics, Hybridization pattern, Hypotonic face, Illkirch cedex, Intermediate alleles, Ivan jeanne weiler, Jamel, Jamel chelly, James macpherson, Jean moulin, John mulley, Judith mallolas, Kennedy institute, Knockout, Large numbers, Laurent, Laurent fries, Laurent villard, Leopold curfs, Leuven, Lille cedex, Linkage analysis, Linkage studies, Lisbeth tranebjaerg, Maarit peippo, Maija castren, Mandel, Marseille cedex, Martine borghgraef, Mathews avenue, Medical genetics, Medical research, Mental retardation, Mental retardation protein fmrp, Michael partington, Microarrays, Microspheres, Mill hill, Minor anomalies, Missense mutation, Molecular basis, Molecular genetics, Molecular studies, Molekulare genetik, Mrna, Mrxs genes, Muscle biopsy, Mutation, Mutation analysis, Mutation detection, Mutation screening, National institute, Netherlands, Netherlands institute, Neuronal plasticity, Nijmegen, Nonspecific xlmr, Normal controls, Novel gene, Oligonucleotides, Other hand, Other populations, Patrick willems, Paul hagerman, Peripheral blood leukocytes, Pietro chiurazzi, Poster, Premutation, Premutation alleles, Premutation carriers, Proc natl acad, Randi hagerman, Research center, Retardation, Retarded individuals, Richard simensen, Roper, Rotterdam, Salisbury district hospital, Salisbury wilts, Salisbury wiltshire, Salvatore adinolfi, Severe language delay, Shorter alleles, Silvia russo, Slight reduction, Spine density, Stanford university, Staten island, Strasbourg cedex, Such arrays, Susan harris, Sylvie jacquot, Syndrome, Syndromic xlmr genes, Tours cedex, Transcriptional activity, Tromso, Trude olsen, Ulrike salat, Unique microspheres, Universita cattolica, Universite laval quebec, University hospital, University hospital leuven, University hospital nijmegen, Victor hugo, Xlmr, Xlmr syndrome, Xlmr syndromes, Yale university, York state institute.
• Teeft :
  • Academic university, Actin cytoskeleton, Actin cytoskeleton organization, Adaptive behavior, Allele, Andre hanauer, Andrea peier, Andrea sharrock, Angela viannamorgante, Balanced translocation, Barbara bardoni, Basic research, Baylor college, Baylor plaza, Belgium, Biological sciences, Bipolar affective disorder, Brain research, Candidate genes, Carola bontekoe, Caroline moore, Cdna, Cdna microarrays, Cedex, Cell lines, Cellular mechanisms, Centre hosp, Charles schwartz, Chelly, Child development unit, Claude moraine, Claude stoll, Claudia bagni, Clinical genetics, Clinical genetics department, Clinical genetics dept, Clinical referrals, Cognitive impairment, Conference report, Corresponding genes, Dana crawford, Daniela toniolo, David nelson, Deletion, Dendritic, Dept, Developmental disabilities, Didier lacombe, Diego otero, Different populations, Elizabeth hinkle, Emory university, Erasmus, Erasmus university, Erasmus university rotterdam, European xlmr consortium, Flora tassone, Fmr1, Fmr1 alleles, Fmr1 gene, Fmr1 gene expression, Fmr1 knockout mice, Fmr1 mrna, Fmr1 mrna expression, Fmr1 mutation, Fmr1 triplets, Fmr2, Fmr2 gene, Fmr2 mutation, Fmrp, Forest hill road, Fragile, Francois rousseau, Frank kooy, Fraxa, Fraxe, Fryns, Full mutation, Full mutation alleles, Fullmutation alleles, Gene, Genet, Genetic background, Genetica, Genetica medica, Genetics, Genetics laboratory, Genetique medicale, Germ cells, Gillian turner, Greenwood, Gregor mendel circle, Hamel, Helger yntema, Herestraat, Histone deacetylases, Hopital saint antoine, Hospital clinic, Human genetics, Hunter genetics, Hybridization pattern, Hypotonic face, Illkirch cedex, Intermediate alleles, Ivan jeanne weiler, Jamel, Jamel chelly, James macpherson, Jean moulin, John mulley, Judith mallolas, Kennedy institute, Knockout, Large numbers, Laurent, Laurent fries, Laurent villard, Leopold curfs, Leuven, Lille cedex, Linkage analysis, Linkage studies, Lisbeth tranebjaerg, Maarit peippo, Maija castren, Mandel, Marseille cedex, Martine borghgraef, Mathews avenue, Medical genetics, Medical research, Mental retardation, Mental retardation protein fmrp, Michael partington, Microarrays, Microspheres, Mill hill, Minor anomalies, Missense mutation, Molecular basis, Molecular genetics, Molecular studies, Molekulare genetik, Mrna, Mrxs genes, Muscle biopsy, Mutation, Mutation analysis, Mutation detection, Mutation screening, National institute, Netherlands, Netherlands institute, Neuronal plasticity, Nijmegen, Nonspecific xlmr, Normal controls, Novel gene, Oligonucleotides, Other hand, Other populations, Patrick willems, Paul hagerman, Peripheral blood leukocytes, Pietro chiurazzi, Poster, Premutation, Premutation alleles, Premutation carriers, Proc natl acad, Randi hagerman, Research center, Retardation, Retarded individuals, Richard simensen, Roper, Rotterdam, Salisbury district hospital, Salisbury wilts, Salisbury wiltshire, Salvatore adinolfi, Severe language delay, Shorter alleles, Silvia russo, Slight reduction, Spine density, Stanford university, Staten island, Strasbourg cedex, Such arrays, Susan harris, Sylvie jacquot, Syndrome, Syndromic xlmr genes, Tours cedex, Transcriptional activity, Tromso, Trude olsen, Ulrike salat, Unique microspheres, Universita cattolica, Universite laval quebec, University hospital, University hospital leuven, University hospital nijmegen, Victor hugo, Xlmr, Xlmr syndrome, Xlmr syndromes, Yale university, York state institute.

Url:

• https://api.istex.fr/document/4659AC135A9DD1BEB7353D4F2A9EB67D3C75FEF2/fulltext/pdf

DOI: 10.1002/1096-8628(20001023)94:5<345::AID-AJMG1>3.0.CO;2-Z

Affiliations:

• Allemagne, Australie, Belgique, Brésil, Canada, France, Géorgie (pays), Norvège, Pays-Bas, Royaume-Uni, États-Unis
• Alsace (région administrative), Aquitaine, Bade-Wurtemberg, Californie, Caroline du Sud, Centre-Val de Loire, Connecticut, District de Tübingen, Grand Est, Gueldre, Hollande-Méridionale, Hollande-Septentrionale, Nouvelle-Aquitaine, Provence-Alpes-Côte d'Azur, Région Centre, Texas, État de New York, État de São Paulo, Île-de-France
• Amsterdam, Bordeaux, Marseille, Nimègue, Paris, Rotterdam, Strasbourg, São Paulo, Tours, Ulm
• Université de São Paulo

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