Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
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.
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.
Pageof 6