-
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
-
2دورية أكاديمية
المؤلفون: Issad Mehdi, Ahossi Victorin, Melli Emma, Hoarau David
المصدر: Journal of Oral Medicine and Oral Surgery, Vol 30, Iss 1, p 1 (2024)
مصطلحات موضوعية: satb2-associated syndrome (sas), glass syndrome, facial dysmorphism, dental anomalies, Dentistry, RK1-715, Surgery, RD1-811
وصف الملف: electronic resource
العلاقة: https://www.jomos.org/articles/mbcb/full_html/2024/01/mbcb230193/mbcb230193.htmlTest; https://doaj.org/toc/2608-1326Test
-
3دورية أكاديمية
المؤلفون: Stacey Bissell, Chris Oliver, Joanna Moss, Mary Heald, Jane Waite, Hayley Crawford, Vishakha Kothari, Lauren Rumbellow, Grace Walters, Caroline Richards
المصدر: Journal of Neurodevelopmental Disorders, Vol 14, Iss 1, Pp 1-21 (2022)
مصطلحات موضوعية: Behavioural phenotype, SATB2-associated syndrome, Autism, Angelman syndrome, Challenging behaviour, Repetitive behaviour, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
وصف الملف: electronic resource
-
4دورية 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
-
5
المؤلفون: Kurosaka, Hiroshi, Yamamoto, Sayuri, Hirasawa, Kyoko, Yanagishita, Tomoe, Fujioka, Kaoru, Yagasaki, Hideaki, Nagata, Miho, Ishihara, Yasuki, Yonei, Ayumi, Asano, Yoshihiro, Nagata, Namiki, Tsujimoto, Takayuki, Inubushi, Toshihiro, Yamamoto, Toshiyuki, Sakai, Norio, Yamashiro, Takashi
المصدر: American Journal of Medical Genetics, Part A. :1-6
مصطلحات موضوعية: craniofacial defect, SATB2-associated syndrome, tooth anomaly
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=jairo_______::158f5a07ca9f1f50b84ea8dde3573518Test
https://hdl.handle.net/11094/91341Test -
6دورية أكاديمية
المؤلفون: Yajie Su, Hui Zhang, Huijun Wang, Bingbing Wu, Jiao Yang, Wenhao Zhou, Long Li
المصدر: Frontiers in Pediatrics, Vol 9 (2021)
مصطلحات موضوعية: MEGDEL syndrome, SATB2-associated syndrome, phenotype, next-generation sequencing, follow-up, Pediatrics, RJ1-570
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fped.2021.713458/fullTest; https://doaj.org/toc/2296-2360Test
-
7دورية أكاديمية
المؤلفون: Yuri A. Zarate, Hilary J. Vernon, Katherine A. Bosanko, Praveen K. Ramani, Murat Gokden, Karin Writzl, Marija Meznaric, Tina Vipotnik Vesnaver, Raghu Ramakrishnaiah, Damjan Osredkar
المصدر: Frontiers in Genetics, Vol 12 (2021)
مصطلحات موضوعية: SATB2, glass syndrome, mitochondrial disease, muscle biopsy, SATB2-Associated syndrome, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fgene.2021.692087/fullTest; https://doaj.org/toc/1664-8021Test
-
8دورية أكاديمية
المؤلفون: Yeqing Qian, Jiao Liu, Yanmei Yang, Min Chen, Chunlei Jin, Penglong Chen, Yongliang Lei, Hangyi Pan, Minyue Dong
المصدر: Frontiers in Genetics, Vol 10 (2019)
مصطلحات موضوعية: SATB2-associated syndrome, chromosome microarray analysis, mosaicism, droplet digital PCR, gap-PCR, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/article/10.3389/fgene.2019.00630/fullTest; https://doaj.org/toc/1664-8021Test
-
9دورية أكاديمية
المؤلفون: Qiong Zhang, Ying Huang, Lei Zhang, Yu-Qiang Ding, Ning-Ning Song
المصدر: Frontiers in Molecular Neuroscience, Vol 12 (2019)
مصطلحات موضوعية: Satb2, cerebral cortex, hippocampus, Satb2-associated syndrome, mouse behavior, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/article/10.3389/fnmol.2019.00033/fullTest; https://doaj.org/toc/1662-5099Test
-
10
المؤلفون: Guilian Sun, Yan-Yan Zhu, Zhiliang Yang
المصدر: World Journal of Clinical Cases
مصطلحات موضوعية: Genetics, business.industry, Mutation (genetic algorithm), Case report, SATB2-associated syndrome, Global developmental delay, Developmental speech and language delay, Medicine, General Medicine, business, Special AT-rich sequence binding protein 2
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14ecee742e8225e73bcd312f31580628Test
http://europepmc.org/articles/PMC8316932Test