Associated Papers
Perthes Disease in a Child With Osteogenesis Imperfecta From a Rare Genetic Variant: A Case Report.
Hong P et al.
Frontiers in Genetics, 2022
Genotypic and Phenotypic Analysis in Chinese Cohort With Autosomal Recessive Osteogenesis Imperfecta.
Li S et al.
Frontiers in Genetics, 2020
The most 5' truncating homozygous mutation of WNT1 in siblings with osteogenesis imperfecta with a variable degree of brain anomalies: a case report.
Kuptanon C et al.
Bmc Medical Genetics, 2018
A systematic review of association studies of common variants associated with idiopathic congenital talipes equinovarus (ICTEV) in humans in the past 30 years.
Yong BC et al.
Springerplus, 2016
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