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https://hdl.handle.net/2440/32541
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Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Kayserili, Hulya | en |
dc.contributor.author | Cox, Timothy Chilton | en |
dc.contributor.author | Cox, Liza L. | en |
dc.contributor.author | Basaran, Seher | en |
dc.contributor.author | Kilic, Gulleyla | en |
dc.contributor.author | Ballabio, Andrea | en |
dc.contributor.author | Yuksel-Apak, Memnune | en |
dc.date.issued | 2001 | en |
dc.identifier.citation | Journal of Medical Genetics, 2001: 38(6):411-417 | en |
dc.identifier.issn | 0022-2593 | en |
dc.identifier.uri | http://hdl.handle.net/2440/32541 | - |
dc.description.statementofresponsibility | Hülya Kayserili, Timothy C Cox, Liza L Cox, Seher Basaran, Gülleyla Kiliç, Andrea Ballabio, Memnune Yüksel-Apak | en |
dc.language.iso | en | en |
dc.publisher | British Medical Journal Publishing Group | en |
dc.rights | © 2001 by the BMJ Publishing Group Ltd. | en |
dc.source.uri | http://jmg.bmj.com/cgi/content/short/38/6/411 | en |
dc.title | Molecular characterisation of a new case of microphthalmia with linear skin defects (MLS) | en |
dc.type | Journal article | en |
dc.contributor.school | School of Molecular and Biomedical Science : Genetics | en |
dc.contributor.organisation | Centre for the Molecular Genetics of Development | en |
dc.identifier.doi | 10.1136/jmg.38.6.411 | en |
Appears in Collections: | Centre for the Molecular Genetics of Development publications Molecular and Biomedical Science publications |
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