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Publication : Expanding the phenotype associated with biallelic WDR60 mutations: Siblings with retinal degeneration and polydactyly lacking other features of short rib thoracic dystrophies.

First Author  Kakar N Year  2018
Journal  Am J Med Genet A Volume  176
Issue  2 Pages  438-442
PubMed ID  29271569 Mgi Id 
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