Finnegan, P., Bourke, J. and O’Connor, C. (2023) “A rare differential for multiple café-au-lait macules: primary microcephaly-3 caused by recessive mutations in CDK5RAP2. Case report and literature review.”, European Journal of Pediatric Dermatology, 33(3), pp. 153-5. doi: 10.26326/2281-9649.33.3.2508.