Xiuli Zhao

Mutations in HOXD13 Underlie Syndactyly Type V and a Novel Brachydactyly-Syndactyly Syndrome

Xiuli Zhao, Miao Sun, Jin Zhao et al. · The American Journal of Human Genetics · 2007 · 105 citations · Full text

Novel Brachydactyly-syndactyly Syndrome, Genetic Disorder, Genetics +4

Mutations of the<i>EPHA2</i>receptor tyrosine kinase gene cause autosomal dominant congenital cataract

Tianxiao Zhang, Rui Hua, Wei Xiao et al. · Human Mutation · 2009 · 101 citations · Full text

Human Ccs, Developmental Biology, Ocular Disease +13

TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model

Jiaqi Liu, Nan Wu, Nan Yang et al. · Genetics in Medicine · 2019 · 89 citations · Full text

Compound Inheritance, Spinal Cord Injury, Congenital Scoliosis +7

Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta

Lulu Li, Bin Mao, Shan Li et al. · Human Mutation · 2019 · 43 citations

Genotypic and Phenotypic Analysis in Chinese Cohort With Autosomal Recessive Osteogenesis Imperfecta

Shan Li, Yixuan Cao, Han Wang et al. · Frontiers in Genetics · 2020 · 40 citations · Full text