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المؤلفون: Miriam Kessi, Jing Peng, Xiaolu Deng, Haolin Duan, Shimeng Chen, Ciliu Zhang, Fei Yin, Fang He, Juan Xiong, Li Yang
المصدر: BMC Medical Genomics
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-9 (2021)مصطلحات موضوعية: Proband, Pediatrics, medicine.medical_specialty, QH426-470, Asymptomatic, Axonogenesis, Loss-of-function, 03 medical and health sciences, Reflex seizure, 0302 clinical medicine, Genotype, Genetics, Medicine, Gender differences, Internal medicine, Genetics (clinical), Loss function, 030304 developmental biology, 0303 health sciences, business.industry, Research, Variants, SYN1, medicine.disease, RC31-1245, Phenotype, Human genetics, Neurodevelopmental Disorders, medicine.symptom, business, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1008e9ee7b18741ec328f1bfc6e25fa8Test
http://europepmc.org/articles/PMC8272254Test -
2دورية أكاديمية
المؤلفون: Juan Xiong, Haolin Duan, Shimeng Chen, Miriam Kessi, Fang He, Xiaolu Deng, Ciliu Zhang, Li Yang, Jing Peng, Fei Yin
المصدر: BMC Medical Genomics, Vol 14, Iss 1, Pp 1-9 (2021)
مصطلحات موضوعية: SYN1, Variants, Neurodevelopmental disorders, Gender differences, Loss-of-function, Internal medicine, RC31-1245, Genetics, QH426-470, edu, anthro-bio
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3دورية أكاديمية
المؤلفون: Xiao‑Liang Xin, Zhi‑Yong Yao, Chaoqun Xing, Zhi Huang, Jing Peng, Yuan‑Wu Liu
المصدر: BMC Medical Genomics; 4/28/2021, Vol. 14 Issue 1, p1-8, 8p