Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Scoliosis and AR[original query] |
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Compound heterozygous mutations of SH3TC2 in Charcot-Marie-Tooth disease type 4C patients. Journal of human genetics 2019 6 64 (9): 961-965. Lee Ah Jin, Nam Soo Hyun, Park Jin-Mo, Kanwal Sumaira, Choi Yu Jin, Lee Hyun Jung, Lee Kyung Suk, Lee Ji Eun, Park Jin-Sung, Choi Byung-Ok, Chung Ki W |
Implication of the SH3TC2 gene in Charcot-Marie-Tooth disease associated with deafness and/or scoliosis: Illustration with four new pathogenic variants. Journal of the neurological sciences 2019 10 406 116376. Lerat J, Magdelaine C, Lunati A, Dzugan H, Dejoie C, Rego M, Beze Beyrie P, Bieth E, Calvas P, Cintas P, Delaubrier A, Demurger F, Gilbert-Dussardier B, Goizet C, Journel H, Laffargue F, Magy L, Taithe F, Toutain A, Urtizberea J A, Sturtz F, Lia A |
Genotypic and Phenotypic Analysis in Chinese Cohort With Autosomal Recessive Osteogenesis Imperfecta. Frontiers in genetics 2020 10 11 984. Li Shan, Cao Yixuan, Wang Han, Li Lulu, Ren Xiuzhi, Mi Huan, Wang Yanzhou, Guan Yun, Zhao Feiyue, Mao Bin, Yang Tao, You Yi, Guan Xin, Yang Yujiao, Zhang Xue, Zhao Xiu |
Lower androgen levels promote abnormal cartilage development in female patients with adolescent idiopathic scoliosis. Annals of translational medicine 2021 7 9 (9): 784. Wu Yuan-Tao, Tang Ming-Xing, Wang Yun-Jia, Li Jiong, Wang Yu-Xiang, Deng Ang, Guo Chao-Feng, Zhang Hong- |
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