المؤلفون: Degenhardt, F., Priebe, L., Lange, C., Hoffmann, P., Meyer-Lindenberg, A., Heinz, A., Walter, H., Lucae, S., Wolf, C., Muller-Myhsok, B., Holsboer, F., Maier, W., Herms, S., Rietschel, M., Nöthen, M.M., Cichon, S., Mattheisen, M., Mühleisen, T., Meier, S., Moebus, S., Strohmaier, J., Gross, M., Breuer, R.

المصدر: American journal of medical genetics / B 159B, 263 - 273 (2012). doi:10.1002/ajmg.b.32034

مصطلحات موضوعية: info:eu-repo/classification/ddc/570, Case-Control Studies, Chromosome Deletion, Chromosomes, Human, Pair 16: genetics, Pair 7: genetics, DNA Copy Number Variations: genetics, Depressive Disorder, Major: genetics, Major: psychology, Gene Duplication: genetics, Genetic Association Studies, Genetic Predisposition to Disease, Genome-Wide Association Study, Germany, Humans, Middle Aged, Phenotype, affective disorder, genome-wide, microdeletion, microduplication, common variants, psy, hist

جغرافية الموضوع: DE

العلاقة: https://juser.fz-juelich.de/record/20236Test

الإتاحة: https://doi.org/10.1002/ajmg.b.32034Test
https://juser.fz-juelich.de/record/20236Test

المؤلفون: Degenhardt, F., Priebe, L., Lange, C., Hoffmann, P., Meyer-Lindenberg, A., Heinz, A., Walter, H., Lucae, S., Wolf, C., Muller-Myhsok, B., Holsboer, F., Maier, W., Herms, S., Rietschel, M., Nöthen, M.M., Cichon, S., Mattheisen, M., Mühleisen, T., Meier, S., Moebus, S., Strohmaier, J., Gross, M., Breuer, R.

المصدر: American journal of medical genetics / B 159B, 263 - 273 (2012). doi:10.1002/ajmg.b.32034

مصطلحات موضوعية: info:eu-repo/classification/ddc/570, Case-Control Studies, Chromosome Deletion, Chromosomes, Human, Pair 16: genetics, Pair 7: genetics, DNA Copy Number Variations: genetics, Depressive Disorder, Major: genetics, Major: psychology, Gene Duplication: genetics, Genetic Association Studies, Genetic Predisposition to Disease, Genome-Wide Association Study, Germany, Humans, Middle Aged, Phenotype, affective disorder, genome-wide, microdeletion, microduplication, common variants

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/pmid:22344817; info:eu-repo/semantics/altIdentifier/wos/WOS:000301175500002; info:eu-repo/semantics/altIdentifier/issn/1552-4841; https://juser.fz-juelich.de/record/20236Test; https://juser.fz-juelich.de/search?p=id:%22PreJuSER-20236%22Test

الإتاحة: https://doi.org/10.1002/ajmg.b.32034Test
https://juser.fz-juelich.de/record/20236Test
https://juser.fz-juelich.de/search?p=id:%22PreJuSER-20236%22Test

المؤلفون: Degenhardt, Franziska, Priebe, Lutz, Lange, Christoph, Hoffmann, Per, Meyer-Lindenberg, Andreas, Heinz, Andreas, Walter, Henrik, Lucae, Susanne, Wolf, Christiane, Müller-Myhsok, Bertram, Holsboer, Florian, Maier, Wolfgang, Herms, Stefan, Rietschel, Marcella, Nöthen, Markus M, Cichon, Sven, Mattheisen, Manuel, Mühleisen, Thomas W, Meier, Sandra, Moebus, Susanne, Strohmaier, Jana, Groß, Magdalena, Breuer, René

المصدر: American journal of medical genetics / B 159B(3), 263-273 (2012). doi:10.1002/ajmg.b.32034

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Case-Control Studies, Chromosome Deletion, Chromosomes, Human, Pair 16: genetics, Pair 7: genetics, DNA Copy Number Variations: genetics, Depressive Disorder, Major: genetics, Major: psychology, Gene Duplication: genetics, Genetic Association Studies, Genetic Predisposition to Disease, Genome-Wide Association Study, Germany, Humans, Middle Aged, Phenotype

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/0148-7299; info:eu-repo/semantics/altIdentifier/issn/1552-485X; info:eu-repo/semantics/altIdentifier/pmid/pmid:22344817; info:eu-repo/semantics/altIdentifier/issn/1552-4841; info:eu-repo/semantics/altIdentifier/issn/1096-8628; https://pub.dzne.de/record/136451Test; https://pub.dzne.de/search?p=id:%22DZNE-2020-02773%22Test

الإتاحة: https://doi.org/10.1002/ajmg.b.32034Test
https://pub.dzne.de/record/136451Test
https://pub.dzne.de/search?p=id:%22DZNE-2020-02773%22Test

المؤلفون: Sutherland, G., Baker, E.

المصدر: http://dx.doi.org/10.1002/1096-8628Test(20000612)96:3%3C429::aid-ajmg37%3E3.0.co;2-f.

مصطلحات موضوعية: Chromosomes, Human, Pair 16, Humans, Chromosome Fragility, Mental Disorders, Chromosome Fragile Sites

العلاقة: American Journal of Medical Genetics Part A, 2000; 96(3):429-429; http://hdl.handle.net/2440/32908Test

الإتاحة: https://doi.org/10.1002/1096-8628Test(20000612)96:3<429::AID-AJMG37>3.0.CO;2-F
https://doi.org/10.1002/1096-8628Test(20000612)96:3%3C429::aid-ajmg37%3E3.0.co;2-f
http://hdl.handle.net/2440/32908Test