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SUTTON, VERNON
One or more keywords matched the following items that are connected to
SUTTON, VERNON
Item Type
Name
Academic Article
DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome.
Concept
Wnt-5a Protein
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.
Search Criteria
Wnt2 Protein