Molecular characterisation of a new case of microphthalmia with linear skin defects (MLS)

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dc.contributor.authorKayserili, Hulyaen
dc.contributor.authorCox, Timothy Chiltonen
dc.contributor.authorCox, Liza L.en
dc.contributor.authorBasaran, Seheren
dc.contributor.authorKilic, Gulleylaen
dc.contributor.authorBallabio, Andreaen
dc.contributor.authorYuksel-Apak, Memnuneen
dc.contributor.organisationCentre for the Molecular Genetics of Developmenten
dc.contributor.schoolSchool of Molecular and Biomedical Science : Geneticsen
dc.date.issued2001en
dc.description.statementofresponsibilityHülya Kayserili, Timothy C Cox, Liza L Cox, Seher Basaran, Gülleyla Kiliç, Andrea Ballabio, Memnune Yüksel-Apaken
dc.identifier.citationJournal of Medical Genetics, 2001: 38(6):411-417en
dc.identifier.doi10.1136/jmg.38.6.411en
dc.identifier.issn0022-2593en
dc.identifier.urihttp://hdl.handle.net/2440/32541
dc.language.isoenen
dc.publisherBritish Medical Journal Publishing Groupen
dc.rights© 2001 by the BMJ Publishing Group Ltd.en
dc.source.urihttp://jmg.bmj.com/cgi/content/short/38/6/411en
dc.titleMolecular characterisation of a new case of microphthalmia with linear skin defects (MLS)en
dc.typeJournal articleen

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