Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/7531
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dc.contributor.authorVan Royen-Kerkhof, A.-
dc.contributor.authorPollthe, B.-
dc.contributor.authorKleijer, W.-
dc.contributor.authorvan Diggelen, O.-
dc.contributor.authorAerts, J.-
dc.contributor.authorHopwood, J.-
dc.contributor.authorBeemer, F.-
dc.date.issued1998-
dc.identifier.citationJournal of Medical Genetics, 1998; 35(11):965-966-
dc.identifier.issn0022-2593-
dc.identifier.issn1468-6244-
dc.identifier.urihttp://hdl.handle.net/2440/7531-
dc.descriptionLetter-
dc.description.statementofresponsibilityRoyen-Kerkhof, van, A. ; Kleijer, W.J. ; Diggelen, van, O.P. ; Aerts, J.M.F.G. ; Hopwoud, J.J. ; Beemer, F.A.-
dc.language.isoen-
dc.publisherBRITISH MED JOURNAL PUBL GROUP-
dc.source.urihttp://jmg.bmj.com/cgi/reprint/35/11/965-
dc.subjectCerebellum-
dc.subjectCells, Cultured-
dc.subjectHumans-
dc.subjectGaucher Disease-
dc.subjectCerebellar Diseases-
dc.subjectSyndrome-
dc.subjectGlucosylceramidase-
dc.subjectPedigree-
dc.subjectChild, Preschool-
dc.subjectInfant-
dc.subjectFemale-
dc.subjectMale-
dc.titleCoexistence of Gaucher-Disease Type 1 and Joubert-Syndrome-
dc.typeJournal article-
dc.identifier.doi10.1136/jmg.35.11.965-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest
Paediatrics publications

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