Author:
Leng YunXia,Lan WeiZhong,Yu KeMing,Liu BingQian,Yang ZhiKuan,Li Zheng,Zhong XingWu,Zhang ShaoChong,Ge Jian
Publisher
Springer Science and Business Media LLC
Subject
General Agricultural and Biological Sciences,General Environmental Science,General Biochemistry, Genetics and Molecular Biology
Reference41 articles.
1. Faivre L, Gorlin R J, Wirtz M K, et al. In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome. J Med Genet, 2003, 40: 34–36 1:CAS:528:DC%2BD3sXht1ymtr8%3D, 10.1136/jmg.40.1.34, 12525539
2. Dietz H C, Cutting G R, Pyeritz R E, et al. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene. Nature, 1991, 352: 337–339 1:CAS:528:DyaK3MXltlegu7w%3D, 10.1038/352337a0, 1852208
3. Knowlton R G, Weaver E J, Struyk A F, et al. Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen gene. Am J Hum Genet 1989, 45: 681–688 1:STN:280:DyaK3c%2FltlGrsQ%3D%3D, 2573273
4. Ojaimi E, Rose K A, Smith W, et al. Methods for a population-based study of myopia and other eye conditions in school children: the Sydney Myopia Study. Ophthalmic Epidemiol, 2005, 12: 59–69 10.1080/09286580490921296, 15848921
5. Morgan I, Rose K. How genetic is school myopia? Prog Retin Eye Res, 2005, 24: 1–38 10.1016/j.preteyeres.2004.06.004, 15555525
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