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Scientific Reports|April 4, 2017
Polymorphism in the Alternative Donor Site of the Cryptic Exon of LHCGR: Functional Consequences and Associations with Testosterone LevelWei Liu, Bing Han, Wenjiao Zhu, et al.Orphanet Journal of Rare Diseases|March 22, 2021
Phenotypic and biochemical characteristics and molecular basis in 36 Chinese patients with androgen receptor variantsHui Zhu, Haijun Yao, Yue Xu, et al.Human Genetics|March 28, 2018
Next-generation sequencing reveals genetic landscape in 46, XY disorders of sexual development patients with variable phenotypesHao Wang, Lele Zhang, Nan Wang, et al.Orphanet Journal of Rare Diseases|December 2, 2024
Clinical spectrum and molecular basis in 19 Chinese patients with 46, XY disorder of sexual development caused by NR5A1 mutationsYue Xu, Xuemeng Liu, Yang Liu, et al.Journal of Medical Genetics|October 17, 2009
Multiple single nucleotide polymorphisms in the human urate transporter 1 (hURAT1) gene are associated with hyperuricaemia in Han ChineseChanggui Li, Lin Han, Albert M Levin, et al.Journal of Cellular and Molecular Medicine|July 5, 2022
PARD3 gene variation as candidate cause of nonsyndromic cleft palate onlyRenjie Cui, Dingli Chen, Na Li, et al.Plos One|January 4, 2014
Genetic heterogeneity of susceptibility gene in different ethnic populations: refining association study of PTPN22 for Graves' disease in a Chinese Han populationLiqiong Xue, Chunming Pan, Zhaohui Gu, et al.Endocrinology|July 9, 2014
Intrinsic expression of a multiexon type 3 deiodinase gene controls zebrafish embryo sizeCuicui Guo, Xia Chen, Huaidong Song, et al.The New England Journal of Medicine|April 4, 2014
Thyroid hormone inactivation in gastrointestinal stromal tumorsMichelle A Maynard, Adrian Marino-Enriquez, Jonathan A Fletcher, et al.Plos Medicine|April 6, 2006
Streptococcal toxic shock syndrome caused by Streptococcus suis serotype 2Jiaqi Tang, Changjun Wang, Youjun Feng, et al.Pageof 6