Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Sotos Syndrome and NFIX[original query] |
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Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features. Journal of human genetics 2012 Mar 57 (3): 207-11. Yoneda Yuriko, Saitsu Hirotomo, Touyama Mayumi, Makita Yoshio, Miyamoto Akie, Hamada Keisuke, Kurotaki Naohiro, Tomita Hiroaki, Nishiyama Kiyomi, Tsurusaki Yoshinori, Doi Hiroshi, Miyake Noriko, Ogata Kazuhiro, Naritomi Kenji, Matsumoto Naomic |
19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndrome. Molecular cytogenetics 2016 9 71. Dong Hai-Yun, Zeng Hui, Hu Yi-Qiao, Xie Li, Wang Jian, Wang Xiu-Ying, Yang Yi-Feng, Tan Zhi-Pi |
Genetic heterogeneity of disorders with overgrowth and intellectual disability: Experience from a center in North India. American journal of medical genetics. Part A 2021 5 185 (8): 2345-2355. Moirangthem Amita, Mandal Kausik, Saxena Deepti, Srivastava Priyanka, Gambhir Poonam Singh, Agrawal Neha, Shambhavi Arya, Nampoothiri Sheela, Phadke Shubha |
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