المؤلفون: Oskarsdottir, Solveig, 1953, Boot, E., Crowley, T. B., Loo, J. C. Y., Arganbright, J. M., Armando, M., Baylis, A. L., Breetvelt, E. J., Castelein, R. M., Chadehumbe, M., Cielo, C. M., de Reuver, S., Eliez, S., Fiksinski, A. M., Forbes, B. J., Gallagher, E., Hopkins, S. E., Jackson, O. A., Levitz-Katz, L., Klingberg, G., Lambert, M. P., Marino, B., Mascarenhas, M. R., Moldenhauer, J., Moss, E. M., Nowakowska, B. A., Orchanian-Cheff, A., Putotto, C., Repetto, G. M., Schindewolf, E., Schneider, M., Solot, C. B., Sullivan, K. E., Swillen, A., Unolt, M., Van Batavia, J. P., Vingerhoets, C., Vorstman, J., Bassett, A. S., McDonald-McGinn, D. M.

المصدر: Genetics in Medicine. 25(3)

مصطلحات موضوعية: Pediatrics, Pediatrik, 22q11, 2 deletion syndrome, Children, Clinical practice guidelines, Review, Treatment, bernard-soulier-syndrome, cardio-facial-syndrome, partial, digeorge-syndrome, obstructive sleep-apnea, live viral vaccines, low-copy repeats, psychiatric-disorders, velocardiofacial syndrome, ocular findings, hearing-loss, Genetics & Heredity

URL الوصول: https://gup.ub.gu.se/publication/331591

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المؤلفون: Davies, R. W., Fiksinski, A. M., Breetvelt, E. J., Williams, N. M., Hooper, S. R., Monfeuga, T., Bassett, A. S., Owen, M. J., Gur, R. E., Morrow, B. E., McDonald-McGinn, D. M., Swillen, A., Chow, E. W. C., van den Bree, M., Emanuel, B. S., Vermeesch, J. R., van Amelsvoort, T., Arango, C., Armando, M., Campbell, L. E., Cubells, J. F., Eliez, S., Garcia-Minaur, S., Gothelf, D., Kates, W. R., Murphy, K. C., Murphy, C. M., Murphy, D. G., Philip, N., Repetto, G. M., Shashi, V., Simon, T. J., Suner, D. H., Vicari, Stefano, Scherer, S. W., Epstein, M. P., Warren, S. T., Morrison, S., Chawner, S., Vingerhoets, C., Breckpot, J., Vergaelen, E., Vogels, A., Monks, S., Prasad, S. E., Sandini, C., Schneider, M., Maeder, J., Fraguas, D., Evers, R., Tassone, F., Morey-Canyelles, J., Ousley, O. Y., Antshel, K. M., Fremont, W., Fritsch, R., Ornstein, C., Daly, E. M., Costain, G. A., Boot, E., Heung, T., Crowley, T. B., Zackai, E. H., Calkins, M. E., Gur, R. C., Mccabe, K. L., Busa, T., Schoch, K., Pontillo, M., Duijff, S. N., Kahn, R. S., Houben, Mariasofia, Kushan, L., Jalbrzikowski, M., Carmel, M., Mekori-Domachevsky, E., Michaelovsky, E., Weinberger, R., Bearden, C. E., Vorstman, J. A. S.

المساهمون: Marseille medical genetics - Centre de génétique médicale de Marseille (MMG), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Département de génétique médicale [Hôpital de la Timone - APHM], Institut National de la Santé et de la Recherche Médicale (INSERM)- Hôpital de la Timone [CHU - APHM] (TIMONE)-Assistance Publique - Hôpitaux de Marseille (APHM)-Aix Marseille Université (AMU), RS: MHeNs - R2 - Mental Health, Psychiatrie & Neuropsychologie, MUMC+: MA Med Staf Spec Psychiatrie (9)

المصدر: Nature Medicine
Nature Medicine, Nature Publishing Group, 2020, 26 (12), pp.1912-1918. ⟨10.1038/s41591-020-1103-1⟩
Nature Medicine, Vol. 26, No 12 (2020) pp. 1912-1918
Nat Med
Nature medicine, vol 26, iss 12
Nature Medicine, 26(12), 1912-1918. Nature Publishing Group

مصطلحات موضوعية: 0301 basic medicine, Male, Multifactorial Inheritance, [SDV]Life Sciences [q-bio], INTELLIGENCE, Medical and Health Sciences, Cohort Studies, ddc:616.89, 0302 clinical medicine, Borderline intellectual functioning, Risk Factors, Intellectual disability, 2.1 Biological and endogenous factors, PREMORBID IQ, Cognitive decline, Aetiology, Child, ComputingMilieux_MISCELLANEOUS, Intelligence quotient, ABNORMALITIES, General Medicine, Middle Aged, Serious Mental Illness, Mental Health, Phenotype, Schizophrenia, 030220 oncology & carcinogenesis, Child, Preschool, Cohort, Female, Clinical psychology, Adult, Psychosis, Adolescent, Immunology, behavioral disciplines and activities, General Biochemistry, Genetics and Molecular Biology, Article, 03 medical and health sciences, Young Adult, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, PSYCHOSIS, Clinical Research, Intellectual Disability, Genetic variation, Behavioral and Social Science, mental disorders, medicine, Genetics, DiGeorge Syndrome, Humans, Cognitive Dysfunction, Preschool, METAANALYSIS, International 22q11.2 Brain and Behavior Consortium, Aged, DECLINE, reliability, business.industry, Prevention, cognitive-development, Genetic Variation, PERFORMANCE, medicine.disease, Brain Disorders, schizophrenia, 030104 developmental biology, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, business

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd71ba11a4a1d3c5766546a6d0c18ebb
https://hal-amu.archives-ouvertes.fr/hal-03222249

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المؤلفون: Vorstman, J. A., Breetvelt, E. J., Hillegers, M. H., Scheepers, F. E.

المصدر: Tijdschrift voor Psychiatrie, 57(12), 928. Uitgeverij Boom

مصطلحات موضوعية: Psychiatry and Mental health, Children and adolescents, Psychotic disorder, Symptoms

وصف الملف: image/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e051f521a6f52025da0b1735026d19ed
https://dspace.library.uu.nl/handle/1874/333776

المؤلفون: Westerveld, H. E., Briet, J. W., Houwaart, E. S., Johan Legemaate, Meerman, Th J. A. M., Breetvelt, E. J., Wall, E.

المساهمون: Public and occupational health

المصدر: Netherlands journal of medicine, 63(9), 368. Bohn, Scheltema & Holkema
Netherlands journal of medicine, 63(9), 368-372. Van Zuiden Communications BV
Scopus-Elsevier

مصطلحات موضوعية: Geneeskunde

وصف الملف: image/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7d4a8859cc8a98766f2b7d04ded3e686
https://dspace.library.uu.nl/handle/1874/21771

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