Family history of von Hippel–Lindau disease was uncommon in Chinese patients: suggesting the higher frequency of de novo mutations in VHL gene in these patients
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/jhg201210.pdf
Reference30 articles.
1. Neumann, H. P. & Wiestler, O. D. Clustering of features of von Hippel-Lindau syndrome: evidence for a complex genetic locus. Lancet 337, 1052–1054 (1991).
2. Maher, E. R., Yates, J. R., Harries, R., Benjamin, C., Harris, R., Moore, A. T. et al. Clinical features and natural history of von Hippel-Lindau disease. Q. J. Med. 77, 1151–1163 (1990).
3. Singh, A. D., Shields, C. L. & Shields, J. A. von Hippel–Lindau Disease. Surv. Ophthalmol. 46, 117–142 (2001).
4. Lonser, R. R., Glenn, G. M., Walther, M., Chew, E. Y., Libutti, S. K., Linehan, W. M. et al. von Hippel-Lindau disease. Lancet 361, 2059–2067 (2003).
5. Maher, E. R., Neumann, H. P. & Richard, S. von Hippel-Lindau disease: a clinical and scientific review. Eur. J. Hum. Genet. 19, 617–623 (2011).
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