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Human Genetics|June 16, 2006
A locus for autosomal dominant accessory auricular anomaly maps to 14q11.2-q12Yongjia Yang, Jihong Guo, Zheng Liu, et al.Scientific Reports|October 14, 2015
SPP2 Mutations Cause Autosomal Dominant Retinitis PigmentosaYuan Liu, Xue Chen, Qihua Xu, et al.American Journal of Human Genetics|November 3, 2009
Autosomal-dominant retinitis pigmentosa caused by a mutation in SNRNP200, a gene required for unwinding of U4/U6 snRNAsChen Zhao, Deepti L Bellur, Shasha Lu, et al.Human Molecular Genetics|January 15, 2014
PRPF4 mutations cause autosomal dominant retinitis pigmentosaXue Chen, Yuan Liu, Xunlun Sheng, et al.JAMA Ophthalmology|January 23, 2015
Molecular genetic testing in clinical diagnostic assessments that demonstrate correlations in patients with autosomal recessive inherited retinal dystrophyXiaoxing Liu, Jingjing Xiao, Hui Huang, et al.Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|January 13, 2025
Clinical practices on acute acquired comitant esotropia: A consensus statement proposed by the Council of Asia-Pacific Strabismus and Pediatric Ophthalmology SocietyWen Wen, Sonal K Farzavandi, Miho Sato, et al.Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|January 9, 2026
Slanted versus conventional bilateral lateral rectus recession in children with convergence insufficiency intermittent exotropia: A multicentre, randomized trialJing Yao, Xiying Wang, Chenhao Yang, et al.Investigative Ophthalmology & Visual Science|March 7, 2013
Targeted sequencing of 179 genes associated with hereditary retinal dystrophies and 10 candidate genes identifies novel and known mutations in patients with various retinal diseasesXuejuan Chen, Kanxing Zhao, Xunlun Sheng, et al.Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|March 7, 2026
International consensuses and guidelines on clinical practices on abducens nerve palsy by the Asia-Pacific Strabismus and Pediatric Ophthalmology Society (APSPOS) and the Academy of Asia-Pacific Professors of Ophthalmology (AAPPO)Jing Yao, Sonal K Farzavandi, Miho Sato, et al.Pageof 6