Cite

    Cori Feist et al.. “Novel compound heterozygous mutations in inositol polyphosphate phosphatase-like 1 in a family with severe opsismodysplasia.” Clinical dysmorphology, vol. 25, no. 4, n.d., p. . http://access.bl.uk/ark:/81055/vdc_100041945961.0x00002e