Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndrome

DC 欄位	值	語言
dc.contributor	生物醫學科學研究所	-
dc.contributor.author	Wang, M.	-
dc.contributor.author	Kishnani, P.	-
dc.contributor.author	Decker-Phillips, M.	-
dc.contributor.author	Kahler, S. G.	-
dc.contributor.author	Chen, Y. T.	-
dc.contributor.author	Godfrey, M.	-
dc.date.accessioned	2020-10-15T01:15:05Z	-
dc.date.available	2020-10-15T01:15:05Z	-
dc.date.issued	1996	-
dc.identifier.issn	http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Drexel&SrcApp=hagerty_opac&KeyRecord=0022-2593&DestApp=JCR&RQ=IF_CAT_BOXPLOT	-
dc.identifier.uri	http://ir.sinica.edu.tw/handle/201000000A/22555	-
dc.description.sponsorship	生物醫學科學研究所	-
dc.language.iso	en	-
dc.relation.ispartof	J Med Genet 33, 760-763	-
dc.title	Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndrome	-
dc.type	journal article	-
dc.identifier.isi	http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=RID&SrcApp=RID&DestLinkType=FullRecord&DestApp=ALL_WOS&KeyUT=A1996VG66200009	-
dc.identifier.url	http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=8880577	-
dc.description.note	已出版;[SCI];沒有審查制度;具代表性	-
item.grantfulltext	none	-
item.cerifentitytype	Publications	-
item.languageiso639-1	en	-
item.openairecristype	http://purl.org/coar/resource_type/c_6501	-
item.fulltext	no fulltext	-
item.openairetype	journal article	-
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