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Public Health Genomics and Precision Health Knowledge Base (v6.0)

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Records 1-6

Query Trace: Cafe-au-Lait Spots and NF1[orginal query]

Diagnostic value of multiple café-au-lait macules for neurofibromatosis 1 in Chinese children. The Journal of dermatology 2015 Oct . Yao Ruen, Wang Lili, Yu Yongguo, Wang Jian, Shen Yipi Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
Clinical and mutational spectrum of neurofibromatosis type 1-like syndrome. JAMA 2009 Nov 302 (19): 2111-8. Messiaen Ludwine, Yao Suxia, Brems Hilde, Callens Tom, Sathienkijkanchai Achara, Denayer Ellen, Spencer Emily, Arn Pamela, Babovic-Vuksanovic Dusica, Bay Carolyn, Bobele Gary, Cohen Bruce H, Escobar Luis, Eunpu Deborah, Grebe Theresa, Greenstein Robert, Hachen Rachel, Irons Mira, Kronn David, Lemire Edmond, Leppig Kathleen, Lim Cynthia, McDonald Marie, Narayanan Vinodh, Pearn Amy, Pedersen Robert, Powell Berkley, Shapiro Lawrence R, Skidmore David, Tegay David, Thiese Heidi, Zackai Elaine H, Vijzelaar Raymon, Taniguchi Koji, Ayada Toranoshin, Okamoto Fuyuki, Yoshimura Akihiko, Parret Annabel, Korf Bruce, Legius Er Similar articles in PubMed
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 Similar articles in PubMed

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