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Article: Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome: Letters to the editor

TitleHemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome: Letters to the editor
Authors
Issue Date1997
PublisherUniversity of Chicago Press. The Journal's web site is located at http://www.journals.uchicago.edu/AJHG
Citation
American journal of human genetics, 1997, v. 61 n. 2, p. 449-452 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/42305
ISSN
2023 Impact Factor: 8.1
2023 SCImago Journal Rankings: 4.516
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorOsborne, LRen_HK
dc.contributor.authorSoder, Sen_HK
dc.contributor.authorShi, XMen_HK
dc.contributor.authorPober, Ben_HK
dc.contributor.authorCosta, Ten_HK
dc.contributor.authorScherer, SWen_HK
dc.contributor.authorTsui, L-Cen_HK
dc.date.accessioned2007-01-08T02:34:09Z-
dc.date.available2007-01-08T02:34:09Z-
dc.date.issued1997en_HK
dc.identifier.citationAmerican journal of human genetics, 1997, v. 61 n. 2, p. 449-452en_HK
dc.identifier.issn0002-9297en_HK
dc.identifier.urihttp://hdl.handle.net/10722/42305-
dc.format.extent138066 bytes-
dc.format.extent30208 bytes-
dc.format.mimetypeapplication/pdf-
dc.format.mimetypeapplication/msword-
dc.languageengen_HK
dc.publisherUniversity of Chicago Press. The Journal's web site is located at http://www.journals.uchicago.edu/AJHGen_HK
dc.rightsAmerican journal of human genetics. Copyright © University of Chicago Press.en_HK
dc.subject.meshAntigens, surface - geneticsen_HK
dc.subject.meshDNA-binding proteins - geneticsen_HK
dc.subject.meshElastin - geneticsen_HK
dc.subject.meshGene deletionen_HK
dc.subject.meshNerve tissue proteins - geneticsen_HK
dc.titleHemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome: Letters to the editoren_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0002-9297&volume=61&issue=2&spage=449&epage=452&date=1997&atitle=Hemizygous+Deletion+of+the+Syntaxin+1A+Gene+in+Individuals+with+Williams+Syndrome:+Letters+to+the+editoren_HK
dc.description.naturepublished_or_final_versionen_HK
dc.identifier.doi10.1086/514850-
dc.identifier.pmid9311751en_HK
dc.identifier.pmcidPMC1715888-
dc.identifier.scopuseid_2-s2.0-0030848775-
dc.identifier.isiWOS:A1997XX70100024-
dc.identifier.issnl0002-9297-

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