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

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Bibliographic Details
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

Description
ISSN:	10184813
DOI:	10.1038/ejhg.2013.263