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1دورية أكاديمية
المؤلفون: Radio F. C., Pang K., Ciolfi A., Levy M. A., Hernandez-Garcia A., Pedace L., Pantaleoni F., Liu Z., de Boer E., Jackson A., Bruselles A., McConkey H., Stellacci E., Lo Cicero S., Motta M., Carrozzo R., Dentici M. L., McWalter K., Desai M., Monaghan K. G., Telegrafi A., Philippe C., Vitobello A., Au M., Grand K., Sanchez-Lara P. A., Baez J., Lindstrom K., Kulch P., Sebastian J., Madan-Khetarpal S., Roadhouse C., MacKenzie J. J., Monteleone B., Saunders C. J., Jean Cuevas J. K., Cross L., Zhou D., Hartley T., Sawyer S. L., Monteiro F. P., Secches T. V., Kok F., Schultz-Rogers L. E., Macke E. L., Morava E., Klee E. W., Kemppainen J., Iascone M., Selicorni A., Tenconi R., Amor D. J., Pais L., Gallacher L., Turnpenny P. D., Stals K., Ellard S., Cabet S., Lesca G., Pascal J., Steindl K., Ravid S., Weiss K., Castle A. M. R., Carter M. T., Kalsner L., de Vries B. B. A., van Bon B. W., Wevers M. R., Pfundt R., Stegmann A. P. A., Kerr B., Kingston H. M., Chandler K. E., Sheehan W., Elias A. F., Shinde D. N., Towne M. C., Robin N. H., Goodloe D., Vanderver A., Sherbini O., Bluske K., Hagelstrom R. T., Zanus C., Faletra F., Musante L., Kurtz-Nelson E. C., Earl R. K., Anderlid B. -M., Morin G., van Slegtenhorst M., Diderich K. E. M., Brooks A. S., Gribnau J., Boers R. G., Finestra T. R., Carter L. B., Rauch A., Gasparini P., Boycott K. M., Barakat T. S., Graham J. M., Faivre L., Banka S., Wang T., Eichler E. E., Priolo M., Dallapiccola B., Vissers L. E. L. M., Sadikovic B., Scott D. A., Holder J. L., Tartaglia M.
المساهمون: Radio, F. C., Pang, K., Ciolfi, A., Levy, M. A., Hernandez-Garcia, A., Pedace, L., Pantaleoni, F., Liu, Z., de Boer, E., Jackson, A., Bruselles, A., Mcconkey, H., Stellacci, E., Lo Cicero, S., Motta, M., Carrozzo, R., Dentici, M. L., Mcwalter, K., Desai, M., Monaghan, K. G., Telegrafi, A., Philippe, C., Vitobello, A., Au, M., Grand, K., Sanchez-Lara, P. A., Baez, J., Lindstrom, K., Kulch, P., Sebastian, J., Madan-Khetarpal, S., Roadhouse, C., Mackenzie, J. J., Monteleone, B., Saunders, C. J., Jean Cuevas, J. K., Cross, L., Zhou, D., Hartley, T., Sawyer, S. L., Monteiro, F. P., Secches, T. V., Kok, F., Schultz-Rogers, L. E., Macke, E. L., Morava, E., Klee, E. W., Kemppainen, J., Iascone, M., Selicorni, A., Tenconi, R., Amor, D. J., Pais, L., Gallacher, L., Turnpenny, P. D., Stals, K., Ellard, S., Cabet, S., Lesca, G., Pascal, J., Steindl, K., Ravid, S., Weiss, K., Castle, A. M. R., Carter, M. T., Kalsner, L., de Vries, B. B. A., van Bon, B. W., Wevers, M. R., Pfundt, R., Stegmann, A. P. A., Kerr, B., Kingston, H. M., Chandler, K. E., Sheehan, W., Elias, A. F., Shinde, D. N., Towne, M. C., Robin, N. H., Goodloe, D., Vanderver, A., Sherbini, O., Bluske, K., Hagelstrom, R. T., Zanus, C., Faletra, F., Musante, L., Kurtz-Nelson, E. C., Earl, R. K., Anderlid, B. -M., Morin, G., van Slegtenhorst, M., Diderich, K. E. M., Brooks, A. S., Gribnau, J., Boers, R. G., Finestra, T. R., Carter, L. B., Rauch, A., Gasparini, P.
مصطلحات موضوعية: 1p36, distal 1p36 deletion syndrome, DNA methylome analysi, episignature, genotype-phenotype correlation, neurodevelopmental disorder, obesity, proximal 1p36 deletion syndrome, SPEN, X chromosome, Adolescent, Autism Spectrum Disorder, Child, Preschool, Chromosome Deletion, Chromosome Disorder, Chromosomes, Human, Pair 1, DNA Methylation, DNA-Binding Protein, Epigenesis, Genetic, Female, Haploinsufficiency, Intellectual Disability, Male, Phenotype, RNA-Binding Protein
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33596411; info:eu-repo/semantics/altIdentifier/wos/WOS:000629143200015; volume:108; issue:3; firstpage:502; lastpage:516; numberofpages:15; journal:AMERICAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/11368/2993648Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85101770406; https://www.sciencedirect.com/science/article/pii/S000292972100015X?via=ihubTest; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008487Test/
الإتاحة: https://doi.org/10.1016/j.ajhg.2021.01.015Test
http://hdl.handle.net/11368/2993648Test
https://www.sciencedirect.com/science/article/pii/S000292972100015X?via=ihubTest
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008487Test/ -
2دورية أكاديمية
المؤلفون: Lugtenberg, D, de Brouwer, A P M, Kleefstra, T, Oudakker, A R, Frints, Suzanna, Schrander-Stumpel, C T R M, Fryns, Jean-Pierre, Jensen, L R, Chelly, J, Moraine, C, Turner, G, Veltman, J A, Hamel, B C J, de Vries, B B A, van Bokhoven, H, Yntema, H G
مصطلحات موضوعية: Chromosome Aberrations, Female, Genome, Human, Haplotypes, Humans, Male, Mental Retardation, X-Linked, Oligonucleotide Array Sequence Analysis, Polymorphism, Genetic, Research Support, Non-U.S. Gov't, Sensitivity and Specificity
العلاقة: Journal of Medical Genetics vol:43 issue:4 pages:362-370; https://lirias.kuleuven.be/handle/123456789/8210Test; http://jmg.bmjjournals.com/cgi/pmidlookup?view=long&pmid=16169931Test
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3دورية أكاديمية
المؤلفون: Kleefstra, T, Smidt, M, Banning, M J G, Oudakker, A R, Van Esch, Hilde, de Brouwer, A P M, Nillesen, W, Sistermans, E A, Hamel, B C J, de Bruijn, D, Fryns, Jean-Pierre, Yntema, H G, Brunner, H G, de Vries, B B A, van Bokhoven, H
مصطلحات موضوعية: Abnormalities, Multiple, Animals, Chromosome Deletion, Chromosomes, Human, Pair 9, Expressed Sequence Tags, Female, Humans, Mental Retardation, Methyltransferases, Mice, Phenotype, Research Support, Non-U.S. Gov't, Syndrome, Telomere, Translocation, Genetic
العلاقة: Journal of Medical Genetics vol:42 issue:4 pages:299-306; https://lirias.kuleuven.be/handle/123456789/7724Test; http://jmg.bmjjournals.com/cgi/pmidlookup?view=long&pmid=15805155Test
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4دورية أكاديمية
المؤلفون: de Vries, B B, Wiegers, A M, Smits, A P, Mohkamsing, S, Duivenvoorden, H J, Fryns, Jean-Pierre, Curfs, L M, Halley, D J, Oostra, B A, van den Ouweland, A M, Niermeijer, M F
مصطلحات موضوعية: Adult, Aged, DNA, Female, Fragile X Syndrome, Humans, Male, Mental Retardation, Mental Status Schedule, Middle Aged, Models, Genetic, Mutation
العلاقة: American Journal of Human Genetics vol:58 issue:5 pages:1025-32; https://lirias.kuleuven.be/handle/123456789/276296Test
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5
المؤلفون: Gilles Morin, Krista Bluske, Nathaniel H. Robin, Laurence Faivre, Manuela Priolo, Dihong Zhou, Evangeline Kurtz-Nelson, Tianyun Wang, Omar Sherbini, Daryl A. Scott, Karen Stals, Fabíola Paoli Monteiro, Kaifang Pang, Sara Cabet, Francesca Clementina Radio, Bruno Dallapiccola, Marjon van Slegtenhorst, Rachel K. Earl, Katheryn Grand, Maria Iascone, Alice S. Brooks, Angelo Selicorni, July K. Jean Cuevas, Paolo Gasparini, Maria Lisa Dentici, Marialetizia Motta, Britt-Marie Anderlid, Kristin Lindstrom, Berrin Monteleone, Andrea Ciolfi, Karin Weiss, Katharina Steindl, Kirsty McWalter, Rosalba Carrozzo, Ruben Boers, Helen Kingston, Kym M. Boycott, Bekim Sadikovic, Laura Schultz-Rogers, Evan E. Eichler, Laura A Cross, Alison M R Castle, Louisa Kalsner, Lucia Pedace, Marijke R. Wevers, John M. Graham, Jessica Sebastian, Antonio Vitobello, Gaetan Lesca, Alexander P.A. Stegmann, Suneeta Madan-Khetarpal, Tahsin Stefan Barakat, Abdallah F. Elias, Teresa Robert Finestra, Adeline Vanderver, Peter D. Turnpenny, Bregje W.M. van Bon, Aida Telegrafi, David J. Amor, Deepali N. Shinde, Pedro A. Sanchez-Lara, Lisenka E.L.M. Vissers, Adam Jackson, Rolph Pfundt, Alessandro Bruselles, Andres Hernandez-Garcia, Karin E. M. Diderich, Flavio Faletra, Dana H. Goodloe, Joanne Baez, Sarit Ravid, Romano Tenconi, Sarah L. Sawyer, Lynn Pais, Bronwyn Kerr, Joost Gribnau, Lauren Carter, Melissa T. Carter, Zhandong Liu, Jennifer L. Kemppainen, Jennifer MacKenzie, Jimmy Holder, Elke de Boer, Margaret Au, Taila Hartley, Carol J Saunders, Luciana Musante, Bert B.A. de Vries, Tania Vertemati Secches, Haley McConkey, Willow Sheehan, Francesca Pantaleoni, Caterina Zanus, Christophe Philippe, Chelsea Roadhouse, Stefania Lo Cicero, Sian Ellard, R. Tanner Hagelstrom, Megha Desai, Fernando Kok, Joset Pascal, Marco Tartaglia, Eric W. Klee, Eva Morava, Michael A. Levy, Peggy Kulch, Lyndon Gallacher, Erica L. Macke, Emilia Stellacci, Siddharth Banka, Kristin G. Monaghan, Anita Rauch, Meghan C. Towne, Kate Chandler
المساهمون: Clinical Genetics, Developmental Biology, Radio, F. C., Pang, K., Ciolfi, A., Levy, M. A., Hernandez-Garcia, A., Pedace, L., Pantaleoni, F., Liu, Z., de Boer, E., Jackson, A., Bruselles, A., Mcconkey, H., Stellacci, E., Lo Cicero, S., Motta, M., Carrozzo, R., Dentici, M. L., Mcwalter, K., Desai, M., Monaghan, K. G., Telegrafi, A., Philippe, C., Vitobello, A., Au, M., Grand, K., Sanchez-Lara, P. A., Baez, J., Lindstrom, K., Kulch, P., Sebastian, J., Madan-Khetarpal, S., Roadhouse, C., Mackenzie, J. J., Monteleone, B., Saunders, C. J., Jean Cuevas, J. K., Cross, L., Zhou, D., Hartley, T., Sawyer, S. L., Monteiro, F. P., Secches, T. V., Kok, F., Schultz-Rogers, L. E., Macke, E. L., Morava, E., Klee, E. W., Kemppainen, J., Iascone, M., Selicorni, A., Tenconi, R., Amor, D. J., Pais, L., Gallacher, L., Turnpenny, P. D., Stals, K., Ellard, S., Cabet, S., Lesca, G., Pascal, J., Steindl, K., Ravid, S., Weiss, K., Castle, A. M. R., Carter, M. T., Kalsner, L., de Vries, B. B. A., van Bon, B. W., Wevers, M. R., Pfundt, R., Stegmann, A. P. A., Kerr, B., Kingston, H. M., Chandler, K. E., Sheehan, W., Elias, A. F., Shinde, D. N., Towne, M. C., Robin, N. H., Goodloe, D., Vanderver, A., Sherbini, O., Bluske, K., Hagelstrom, R. T., Zanus, C., Faletra, F., Musante, L., Kurtz-Nelson, E. C., Earl, R. K., Anderlid, B. -M., Morin, G., van Slegtenhorst, M., Diderich, K. E. M., Brooks, A. S., Gribnau, J., Boers, R. G., Finestra, T. R., Carter, L. B., Rauch, A., Gasparini, P., Boycott, K. M., Barakat, T. S., Graham, J. M., Faivre, L., Banka, S., Wang, T., Eichler, E. E., Priolo, M., Dallapiccola, B., Vissers, L. E. L. M., Sadikovic, B., Scott, D. A., Holder, J. L., Tartaglia, M., MUMC+: DA KG Lab Centraal Lab (9), RS: FHML non-thematic output
المصدر: American Journal of Human Genetics, 108(3), 502-516. Cell Press
American Journal of Human Genetics, 108, 3, pp. 502-516
Am J Hum Genet
American Journal of Human Genetics, 108, 502-516مصطلحات موضوعية: 0301 basic medicine, SHARP, Male, obesity, genotype-phenotype correlations, Autism Spectrum Disorder, PROTEIN, Chromosome Disorders, Haploinsufficiency, RNA-Binding Protein, PHENOTYPE CORRELATIONS, 1p36, distal 1p36 deletion syndrome, DNA methylome analysis, episignature, neurodevelopmental disorder, proximal 1p36 deletion syndrome, SPEN, X chromosome, Adolescent, Child, Child, Preschool, Chromosome Deletion, Chromosomes, Human, Pair 1, Chromosomes, Human, X, DNA Methylation, DNA-Binding Proteins, Epigenesis, Genetic, Female, Humans, Intellectual Disability, Neurodevelopmental Disorders, Phenotype, RNA-Binding Proteins, Young Adult, 0302 clinical medicine, Neurodevelopmental disorder, Neurodevelopmental Disorder, Intellectual disability, MOLECULAR CHARACTERIZATION, Genetics (clinical), Genetics, DNA methylome analysi, SPLIT-ENDS, Hypotonia, Autism spectrum disorder, MONOSOMY 1P36, Pair 1, medicine.symptom, Rare cancers Radboud Institute for Health Sciences [Radboudumc 9], Human, DNA-Binding Protein, Biology, genotype-phenotype correlation, Chromosomes, 03 medical and health sciences, Genetic, SDG 3 - Good Health and Well-being, Report, REVEALS, medicine, Epigenetics, Preschool, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], 1p36 deletion syndrome, IDENTIFICATION, MUTATIONS, medicine.disease, GENE, 030104 developmental biology, Chromosome Disorder, 030217 neurology & neurosurgery, Epigenesis
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ca1a210d6320f77ca12d03a0549f6d7Test
https://pure.eur.nl/en/publications/6c5a2968-0de0-4074-8849-a2d72291e184Test