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1دورية أكاديمية
المؤلفون: Xiaojing Li, Xiaowei Ye, Jimei Su
المصدر: BMC Oral Health, Vol 22, Iss 1, Pp 1-5 (2022)
مصطلحات موضوعية: SATB2-associated syndrome, SATB2 gene, Dental abnormalities, Dentistry, RK1-715
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/1472-6831Test
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2دورية أكاديميةAdvantages of Augmentative and Alternative Communication Use in Individuals with SATB2 Gene Mutation
المؤلفون: Brisker, Regan
المصدر: 2023 SLP Posters
مصطلحات موضوعية: SATB2 gene mutation, SATB2-associated syndrome, Augmentative Alternative Communication, AAC, Communication Sciences and Disorders, Speech and Hearing Science, Speech Pathology and Audiology
وصف الملف: application/pdf
العلاقة: https://griffinshare.fontbonne.edu/slp-posters-2023/11Test; https://griffinshare.fontbonne.edu/context/slp-posters-2023/article/1010/viewcontent/ua_cdde_projects_2023_Brisker.pdfTest
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3تقرير
المصدر: Journal of International Medical Research, vol. 44, no. 2, pp. 395-402, 2016. ; ISSN: 0300-0605
مصطلحات موضوعية: 2q32q33 microdeletion syndrome, behavioural problems, secondary cognitive decline, developmental delay, SATB2 gene, mikrodelecijski sindrom 2q32q33, vedenjski problemi, mikrodelecija, sindrom, sekundarni upad kognitivnih sposobnosti, zaostanek v razvoju, gen SATB2, info:eu-repo/classification/udc/575
وصف الملف: application/pdf; text/url
العلاقة: info:eu-repo/semantics/altIdentifier/pissn/0300-0605; https://dk.um.si/IzpisGradiva.php?id=66848Test; https://dk.um.si/Dokument.php?id=114130&dnTest=; https://dk.um.si/Dokument.php?id=114129&dnTest=; https://plus.si.cobiss.net/opac7/bib/5609791?lang=slTest
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المصدر: The Journal of International Medical Research
مصطلحات موضوعية: Adult, 0301 basic medicine, Hysteria, Chromosome Breakpoints, Case Report, 030105 genetics & heredity, Biology, Biochemistry, Myosin Type I, 03 medical and health sciences, Glutaminase, Intellectual Disability, Intellectual disability, medicine, Humans, Abnormalities, Multiple, Cognitive Dysfunction, Cognitive decline, Gene, Genetics, Biochemistry (medical), Breakpoint, SATB2 gene, Membrane Proteins, Karyotype, Matrix Attachment Region Binding Proteins, Cell Biology, General Medicine, Microdeletion syndrome, secondary cognitive decline, medicine.disease, Phenotype, Phosphoric Monoester Hydrolases, Neoplasm Proteins, developmental delay, Aggression, 030104 developmental biology, Chromosomes, Human, Pair 2, Karyotyping, 2q32q33 microdeletion syndrome, Female, Chromosome Deletion, behavioural problems, Self-Injurious Behavior, Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dc4efc0c5b816c92d4a8b1d1ec12f88Test
https://doi.org/10.1177/0300060515595651Test