Cite
MLA Citation
Naseebullah Kakar et al.. “Expanding the phenotype associated with biallelic WDR60 mutations: Siblings with retinal degeneration and polydactyly lacking other features of short rib thoracic dystrophies.” American journal of medical genetics, vol. 176, no. 2, 2018, pp. 438–442. http://access.bl.uk/ark:/81055/vdc_100055779531.0x000019