Disease: Robinow syndrome- autosomal recessive
- <em>ROR2</em>-Related Robinow Syndrome
- A homozygous ROR2 variant in a family with atypical Robinow syndrome and tetramelic transverse deficiency of autopods
- A very rare syndrome and its rare urological complication: Incomplet bladder duplication in Robinow syndrome
- Autosomal recessive Robinow syndrome with novel ROR2 variants: distinct cases exhibiting the clinical variability
- Clinical and molecular characterization of four patients with Robinow syndrome from different families
- Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations
- Craniofacial and intraoral phenotype of Robinow syndrome forms
- Disruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B
- Extremity anomalies associated with Robinow syndrome
- Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome
- Identification of novel ROR2 gene mutations in Indian children with Robinow syndrome
- Mechanistic studies in Drosophila and chicken give new insights into functions of DVL1 in dominant Robinow syndrome
- Nephrological and urological symptoms in patients with Robinow syndrome - a report of two cases
- Neurocognitive, adaptive, and psychosocial functioning in individuals with Robinow syndrome
- Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome
- Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability
- Phenotypic and mutational spectrum of ROR2-related Robinow syndrome
- Prenatal diagnosis of ROR-2 related Robinow syndrome presenting with fetal ultrasound findings of mesomelia, vertebral, digital and genital abnormalities
- Robinow syndrome in an extremely preterm infant: Novel homozygous ROR2 variant detected by rapid exome sequencing
- Tomographic Study of the Malformation Complex in Correlation With the Genotype in Patients With Robinow Syndrome: Review Article
- Whole-exome sequencing identified compound heterozygous variants in ROR2 gene in a fetus with Robinow syndrome