المؤلفون: Mackay Deborah J.G., Eggermann Thomas, Buiting Karin, Garin Intza, Netchine Irène, Linglart Agnès, de Nanclares Guiomar Perez

المصدر: Biomolecular Concepts, Vol 6, Iss 1, Pp 47-57 (2015)

مصطلحات موضوعية: angelman syndrome, beckwith-wiedemann syndrome, imprinting disorder, multilocus methylation defect, prader-willis syndrome, pseudohypoparathyroidism type 1b, silver-russell syndrome, temple syndrome, transient neonatal diabetes, wang-kagami-ogata syndrome, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1868-5021; https://doaj.org/toc/1868-503X

URL الوصول: https://doaj.org/article/f4bb39fe19704f8686920ef63fe2b309

المؤلفون: Thomas Eggermann, Agnès Linglart, Deborah J G Mackay, Irène Netchine, Karin Buiting, Intza Garin, Guiomar Perez de Nanclares

المصدر: Biomolecular Concepts, Vol 6, Iss 1, Pp 47-57 (2015)

مصطلحات موضوعية: QH301-705.5, Medizin, Epigenetics of autism, Biology, General Biochemistry, Genetics and Molecular Biology, Genomic Imprinting, Cellular and Molecular Neuroscience, Angelman syndrome, medicine, Animals, Chromosomes, Human, Humans, angelman syndrome, Biology (General), Allele, Imprinting (psychology), pseudohypoparathyroidism type 1b, Gene, beckwith-wiedemann syndrome, imprinting disorder, Genetics, wang-kagami-ogata syndrome, Genetic Diseases, Inborn, silver-russell syndrome, General Medicine, Methylation, DNA Methylation, medicine.disease, transient neonatal diabetes, Genetic Loci, DNA methylation, multilocus methylation defect, prader-willis syndrome, Genomic imprinting, temple syndrome

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9025a4ed65154d84dc65da47302f6bd5
https://doi.org/10.1515/bmc-2014-0037