Disease: Spondyloepiphyseal dysplasia- Omani type
- A Chinese case of CHST3-related skeletal dysplasia and a systematic review
- A novel nonsense mutation in CHST3 in a Turkish patient with spondyloepiphyseal dysplasia, Omani type
- Autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia and distinctive facial appearance
- Benzene ring bisphenol A substitutes potently inhibit human, rat, and mouse gonadal 3β-hydroxysteroid dehydrogenases: Structure-activity relationship and in silico docking analysis
- Chondrodysplasia with multiple dislocations: comprehensive study of a series of 30 cases
- CHST3-related skeletal dysplasia in 14 patients: Identification of 8 novel variants and further expansion of the phenotypic spectrum
- Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis
- Intrafamilial variability and neurological manifestations in two siblings with carbohydrate sulfotransferase 3-related skeletal dysplasia
- Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26
- Loss of chondroitin 6-O-sulfotransferase-1 function results in severe human chondrodysplasia with progressive spinal involvement
- Omani-type spondyloepiphyseal dysplasia with cardiac involvement caused by a missense mutation in CHST3
- Posterior Circulation Stroke due to Atlantoaxial Instability in CHST3-Related Skeletal Dysplasia: A Case Report
- Spondyloepiphyseal dysplasia Omani type: a new recessive type of SED with progressive spinal involvement
- Spondyloepiphyseal dysplasia Omani type: CHST3 mutation spectrum and phenotypes in three Indian families
- Spondyloepiphyseal dysplasia, Omani type: further definition of the phenotype
- Subclinical hypothyroidism in children and adolescents as mild dysfunction of the thyroid gland: a single-center study
- Two Somali half-siblings with CHST3-related chondrodysplasia illustrating the phenotypic spectrum and intrafamilial variability