{"identifier":"nobleid:/w1/20260526/8A467D20","arkIdentifier":"ark:/48914/w1/20260526/8A467D20","version":1,"workTitle":"Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations.","workType":"Journal Article","authors":"Robitaille JM, Gillett RM, LeBlanc MA, Gaston D, Nightingale M, Mackley MP, Parkash S, Hathaway J, Thomas A, Ells A","description":null,"workUrl":null,"createdAt":"2026-05-26T03:30:10.692198Z","canonicalUrl":"https://nobleid.org/ark:/48914/w1/20260526/8A467D20.v1"}