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Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.

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Title: Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.
Authors: Jones, Gabriela E1, Ostergaard, Pia2, Moore, Anthony T3, Connell, Fiona C4, Williams, Denise5, Quarrell, Oliver6, Brady, Angela F7, Spier, Isabel8, Hazan, Filiz9, Moldovan, Oana10, Wieczorek, Dagmar11, Mikat, Barbara11, Petit, Florence12, Coubes, Christine13, Saul, Robert A14, Brice, Glen15, Gordon, Kristiana16, Jeffery, Steve2, Mortimer, Peter S16, Vasudevan, Pradeep C1
Source: European Journal of Human Genetics. Jul2014, Vol. 22 Issue 7, p881-887. 7p.
Database: Academic Search Ultimate
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  Data: Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.
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  Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Human+Genetics%22">European Journal of Human Genetics</searchLink>. Jul2014, Vol. 22 Issue 7, p881-887. 7p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=96423865
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