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Article: Identification of two mutations (S50Y and 4173delC) in the CFTR gene from patients with congenital bilateral absence of vas deferens (CBAVD)

TitleIdentification of two mutations (S50Y and 4173delC) in the CFTR gene from patients with congenital bilateral absence of vas deferens (CBAVD)
Authors
Issue Date1997
PublisherJohn Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/38515
Citation
Human Mutation, 1997, v. 9 n. 2, p. 183-184 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/133886
ISSN
2015 Impact Factor: 5.089
2015 SCImago Journal Rankings: 3.670
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorZielenski, Jen_HK
dc.contributor.authorPatrizio, Pen_HK
dc.contributor.authorMarkiewicz, Den_HK
dc.contributor.authorAsch, RHen_HK
dc.contributor.authorTsui, LCen_HK
dc.date.accessioned2011-06-03T06:10:22Z-
dc.date.available2011-06-03T06:10:22Z-
dc.date.issued1997en_HK
dc.identifier.citationHuman Mutation, 1997, v. 9 n. 2, p. 183-184en_HK
dc.identifier.issn1059-7794en_HK
dc.identifier.urihttp://hdl.handle.net/10722/133886-
dc.languageeng-
dc.publisherJohn Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/38515en_HK
dc.relation.ispartofHuman Mutationen_HK
dc.rightsHuman mutation. Copyright © John Wiley & Sons, Inc.-
dc.subject.meshCongenital Abnormalities - genetics-
dc.subject.meshCystic Fibrosis - complications - genetics-
dc.subject.meshCystic Fibrosis Transmembrane Conductance Regulator - genetics-
dc.subject.meshMutation - genetics-
dc.subject.meshVas Deferens - abnormalities-
dc.titleIdentification of two mutations (S50Y and 4173delC) in the CFTR gene from patients with congenital bilateral absence of vas deferens (CBAVD)en_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1059-7794&volume=9&issue=2&spage=183&epage=184&date=1997&atitle=Identification+of+two+mutations+(S50Y+and+4173delC)+in+the+CFTR+gene+from+patients+with+congenital+bilateral+absence+of+vas+deferens+(CBAVD)-
dc.identifier.emailTsui, LC: tsuilc@hkucc.hku.hken_HK
dc.identifier.authorityTsui, LC=rp00058en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/(SICI)1098-1004(1997)9:2<183::AID-HUMU13>3.0.CO;2-Zen_HK
dc.identifier.pmid9067761-
dc.identifier.scopuseid_2-s2.0-0030950520en_HK
dc.identifier.hkuros121044-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0030950520&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume9en_HK
dc.identifier.issue2en_HK
dc.identifier.spage183en_HK
dc.identifier.epage184en_HK
dc.identifier.isiWOS:A1997WK78500013-
dc.publisher.placeUnited Statesen_HK
dc.identifier.scopusauthoridZielenski, J=7003732699en_HK
dc.identifier.scopusauthoridPatrizio, P=7004465395en_HK
dc.identifier.scopusauthoridMarkiewicz, D=7007146509en_HK
dc.identifier.scopusauthoridAsch, RH=35593760800en_HK
dc.identifier.scopusauthoridTsui, LC=7102754167en_HK

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