Robinow Syndrome Baby
Jan. 12, 2025
Robinow syndrome: MedlinePlus Genetics Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome. | Semantic Scholar DVL3 Alleles Resulting in a −1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome - ScienceDirect Robinow Syndrome Baby
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