Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/5848
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dc.contributor.authorGuldberg, P.-
dc.contributor.authorRey, F.-
dc.contributor.authorZschocke, J.-
dc.contributor.authorRomano, V.-
dc.contributor.authorFRANCOIS, Baudouin-
dc.contributor.authorMICHIELS, Luc-
dc.contributor.authorUllrich, K.-
dc.contributor.authorHoffmann, G.-
dc.contributor.authorBurgard, P.-
dc.contributor.authorSchmidt, H.-
dc.contributor.authorMeli, C.-
dc.contributor.authorRiva, E.-
dc.contributor.authorDianzani, I.-
dc.contributor.authorPonzone, A.-
dc.contributor.authorRey, J.-
dc.contributor.authorGüttler, F.-
dc.date.accessioned2007-12-20T16:02:37Z-
dc.date.available2007-12-20T16:02:37Z-
dc.date.issued1998-
dc.identifier.citationThe American journal of human genetics, 63. p. 71-79-
dc.identifier.urihttp://hdl.handle.net/1942/5848-
dc.titleA European multi-center study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype-
dc.typeJournal Contribution-
dc.identifier.epage79-
dc.identifier.spage71-
dc.identifier.volume63-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.bibliographicCitation.oldjcatA1-
dc.identifier.isi000074761000012-
item.validationecoom 1999-
item.fulltextNo Fulltext-
item.contributorGuldberg, P.-
item.contributorRey, F.-
item.contributorZschocke, J.-
item.contributorRomano, V.-
item.contributorFRANCOIS, Baudouin-
item.contributorMICHIELS, Luc-
item.contributorUllrich, K.-
item.contributorHoffmann, G.-
item.contributorBurgard, P.-
item.contributorSchmidt, H.-
item.contributorMeli, C.-
item.contributorRiva, E.-
item.contributorDianzani, I.-
item.contributorPonzone, A.-
item.contributorRey, J.-
item.contributorGüttler, F.-
item.accessRightsClosed Access-
item.fullcitationGuldberg, P.; Rey, F.; Zschocke, J.; Romano, V.; FRANCOIS, Baudouin; MICHIELS, Luc; Ullrich, K.; Hoffmann, G.; Burgard, P.; Schmidt, H.; Meli, C.; Riva, E.; Dianzani, I.; Ponzone, A.; Rey, J. & Güttler, F. (1998) A European multi-center study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype. In: The American journal of human genetics, 63. p. 71-79.-
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