Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/5202
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dc.contributor.authorMICHIELS, Luc-
dc.contributor.authorFRANCOIS, Baudouin-
dc.contributor.authorRAUS, Jef-
dc.contributor.authorVANDEVYVER, CAROLINE-
dc.date.accessioned2007-12-20T15:56:34Z-
dc.date.available2007-12-20T15:56:34Z-
dc.date.issued1996-
dc.identifier.citationJournal of inherited metabolic disease, 19(6). p. 735-738-
dc.identifier.issn0141-8955-
dc.identifier.urihttp://hdl.handle.net/1942/5202-
dc.description.abstractA system of five sets of multiplex polymerase chain reaction amplifications followed by denaturing gel electrophoresis analysis allows rapid analysis of all 13 exons of the phenylalanine hydroxylase gene.-
dc.language.isoen-
dc.titleRapid identification of PKU-associated mutations by multiplex DGGE analysis of the PAG gene-
dc.typeJournal Contribution-
dc.identifier.epage738-
dc.identifier.issue6-
dc.identifier.spage735-
dc.identifier.volume19-
local.type.refereedRefereed-
dc.bibliographicCitation.oldjcat-
dc.identifier.doi10.1007/BF01799164-
item.fulltextNo Fulltext-
item.contributorMICHIELS, Luc-
item.contributorFRANCOIS, Baudouin-
item.contributorRAUS, Jef-
item.contributorVANDEVYVER, CAROLINE-
item.fullcitationMICHIELS, Luc; FRANCOIS, Baudouin; RAUS, Jef & VANDEVYVER, CAROLINE (1996) Rapid identification of PKU-associated mutations by multiplex DGGE analysis of the PAG gene. In: Journal of inherited metabolic disease, 19(6). p. 735-738.-
item.accessRightsClosed Access-
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