Records 1 - 4
| 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