HuGE Literature Finder
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Molecular Characterization of NF1 and Neurofibromatosis Type 1 Genotype-Phenotype Correlations in a Chinese Population. Scientific reports 2015 5 11291. Zhang Jia, Tong Hanxing, Fu Xi'an, Zhang Yong, Liu Jiangbo, Cheng Ruhong, Liang Jianying, Peng Jie, Sun Zhonghui, Liu Hong, Zhang Furen, Lu Weiqi, Li Ming, Yao Zhiro |
Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations? Human genomics 2012 6 (1): 1. Alkindy A, Chuzhanova N, Kini U, Cooper DN, Upadhyaya M |
Absence of exon 17 c.2970-2872delAAT mutation in Turkish NF1 patients with mild phenotype. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2011 Dec 27 (12): 2113-6. Terzi Yunus Kasim, Sirin Burcu, Serdaroglu Esra, Anlar Banu, Aysun Sabiha, Hosgor Guzen, Arslan Elif Acar, Ayter Sukri |
Exonic deletions in the NF1 gene in patients with neurofibromatosis type I from the lower Silesian region of Poland. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 0 23 (4): 517-21. Laczma?ska Izabela, Szczepaniak Ma?gorzata, Jakubiak Aleksandra, Stembalska Agniesz |
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- Page last updated:Jun 28, 2022
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