Attitudes toward genetic diagnosis and prenatal diagnosis of X-linked Alport syndrome in China
Author:
Publisher
Wiley
Subject
Nephrology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-1797.2012.01562.x/fullpdf
Reference20 articles.
1. Autosomal dominant progressive nephropathy with deafness: Linkage to a new locus on chromosome 11q24;Prakash;J. Am. Soc. Nephrol.,2003
2. Clinical and genetic aspects of Alport syndrome;Golshayan;Rev. Med. Suisse,2006
3. Structure of the human type IV collagen gene COL4A3 and mutations in autosomal Alport syndrome;Heidet;J. Am. Soc. Nephrol.,2001
4. COL4A3/COL4A4 mutations: From familial hematuria to autosomal-dominant or recessive Alport syndrome;Longo;Kidney Int.,2002
5. Novel COL4A5, COL4A4, and COL4A3 mutations in Alport syndrome;Nagel;Hum. Mutat.,2005
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Temporal retinal thinning might be an early diagnostic indicator in male pediatric X-linked Alport syndrome;International Journal of Ophthalmology;2022-07-18
2. Case Report: Preimplantation Genetic Testing and Pregnancy Outcomes in Women With Alport Syndrome;Frontiers in Genetics;2021-02-09
3. Prenatal diagnostic services in three regional centers in Vietnam;International Journal of Public Health;2016-09-15
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