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BMC Oral Health|September 27, 2025
A novel phex gene variant causes non-syndromic tooth agenesisYuhua Pan, Bingqiang Hua, He Wang, et al.
Clinical Oral Investigations|May 31, 2022
Identification of a novel missense heterozygous mutation in the KDF1 gene for non-syndromic congenital anodontiaYuhua Pan, Sheng Yi, Dong Chen, et al.
Neuromuscular Disorders : NMD|March 20, 2021
A rare case of monozygotic triplets with Duchenne muscular dystrophyLiang Wang, Jinfu Lin, Fu Xiong, et al.
BMC Medical Genomics|July 8, 2024
Four novel mutations identified in the COL4A3, COL4A4 and COL4A5 genes in 10 families with Alport syndromeDuocai Wang, Meize Pan, Hang Li, et al.
European Journal of Oral Sciences|January 4, 2023
A novel single-base deletion of the RUNX Family Transcription Factor 2 gene associated with cleidocranial dysplasiaYuhua Pan, Wanyu Lu, Weidong Meng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 9, 2010
[Analysis of the phenotype-genotype relationship of Hb Constant Spring]Man-na Sun, Fu Xiong, Xin-hua Zhang, et al.
Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University|March 21, 2006
[Establishment of transgenic mouse model of familial amyotrophic lateral sclerosis and identification of the filial generation]Hui Huang, Cheng Zhang, Jing Xi, et al.
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