Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfectaFang Lv, Mei Li, Xiaojie Xu et al.|Journal of Human Genetics|2016Cited by 43
Zoledronic Acid Versus Alendronate In The Treatment of Children With Osteogenesis Imperfecta: A 2-Year Clinical StudyFang Lv, Mei Li, Yi Liu et al.|Endocrine Practice|2018Cited by 27
Novel Mutations in PLOD2 Cause Rare Bruck SyndromeFang Lv, Mei Li, Xiaojie Xu et al.|Calcified Tissue International|2017Cited by 26
Novel Mutations in SERPINF1 Result in Rare Osteogenesis Imperfecta Type VIJianyi Wang, Mei Li, Yi Liu et al.|Calcified Tissue International|2016Cited by 24
Genotype-phenotype analysis of a rare type of osteogenesis imperfecta in four Chinese families with WNT1 mutationsYi Liu, Mei Li, Lijie Song et al.|Clinica Chimica Acta|2016Cited by 24