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SUTTON, VERNON
One or more keywords matched the following items that are connected to
SUTTON, VERNON
Item Type
Name
Concept
Dwarfism
Academic Article
DVL1 frameshift mutations clustering in the penultimate exon cause autosomal-dominant Robinow syndrome.
Academic Article
DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome.
Academic Article
WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome.
Academic Article
Biallelic and De Novo Variants in DONSON Reveal a Clinical Spectrum of Cell Cycle-opathies with Microcephaly, Dwarfism and Skeletal Abnormalities.
Academic Article
Characterization of the Robinow syndrome skeletal phenotype, bone micro-architecture, and genotype-phenotype correlations with the osteosclerotic form.
Academic Article
Neurocognitive, adaptive, and psychosocial functioning in individuals with Robinow syndrome.
Academic Article
Extremity anomalies associated with Robinow syndrome.
Academic Article
Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome.
Academic Article
Craniofacial phenotypes associated with Robinow syndrome.
Academic Article
Phenotypic and mutational spectrum of ROR2-related Robinow syndrome.
Search Criteria
Dwarfism