Disease: Lymphedema- microcephaly and chorioretinopathy syndrome
- A novel KIF11 mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous family
- A Novel Mutation of <em>KIF11</em> in a Child with 22q11.2 Deletion Syndrome Associated with MCLMR
- A Novel Mutation of KIF11 in a Child with 22q11.2 Deletion Syndrome Associated with MCLMR
- Autosomal Dominant Microcephaly Associated With Congenital Lymphedema and Chorioretinopathy Due to a Novel Mutation in KIF11
- Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: five novel mutations and review of the literature
- Congenital toxoplasmosis mimicking microcephaly-lymphedema-chorioretinal dysplasia
- Eg5 and Diseases: From the Well-Known Role in Cancer to the Less-Known Activity in Noncancerous Pathological Conditions
- KIF11 microdeletion is associated with microcephaly, chorioretinopathy and intellectual disability
- Loss-of-function of kinesin-5 KIF11 causes microcephaly, chorioretinopathy, and developmental disorders through chromosome instability and cell cycle arrest
- Microcephaly with chorioretinopathy in a brother-sister pair: evidence for germ line mosaicism and further delineation of the ocular phenotype
- Microcephaly-chorioretinopathy syndrome, autosomal recessive form. A case report
- Microcephaly-lymphedema-chorioretinal dysplasia associated with pachymicrogyria and atrophy of the cerebellar vermis: an integration of brain-ocular migration disorders
- Microcephaly, lymphedema, chorioretinopathy and atrial septal defect: a case report and review of the literature
- Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy
- No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome
- Novel variant of KIF11 associated with MCLMR syndrome
- Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations in KIF11
- Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations