File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1002/(SICI)1098-1004(1997)9:2<183::AID-HUMU13>3.0.CO;2-Z
- Scopus: eid_2-s2.0-0030950520
- PMID: 9067761
- WOS: WOS:A1997WK78500013
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Identification of two mutations (S50Y and 4173delC) in the CFTR gene from patients with congenital bilateral absence of vas deferens (CBAVD)
Title | Identification of two mutations (S50Y and 4173delC) in the CFTR gene from patients with congenital bilateral absence of vas deferens (CBAVD) |
---|---|
Authors | |
Issue Date | 1997 |
Publisher | John 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 Identifier | http://hdl.handle.net/10722/133886 |
ISSN | 2023 Impact Factor: 3.3 2023 SCImago Journal Rankings: 1.686 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Zielenski, J | en_HK |
dc.contributor.author | Patrizio, P | en_HK |
dc.contributor.author | Markiewicz, D | en_HK |
dc.contributor.author | Asch, RH | en_HK |
dc.contributor.author | Tsui, LC | en_HK |
dc.date.accessioned | 2011-06-03T06:10:22Z | - |
dc.date.available | 2011-06-03T06:10:22Z | - |
dc.date.issued | 1997 | en_HK |
dc.identifier.citation | Human Mutation, 1997, v. 9 n. 2, p. 183-184 | en_HK |
dc.identifier.issn | 1059-7794 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/133886 | - |
dc.language | eng | - |
dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/38515 | en_HK |
dc.relation.ispartof | Human Mutation | en_HK |
dc.rights | Human mutation. Copyright © John Wiley & Sons, Inc. | - |
dc.subject.mesh | Congenital Abnormalities - genetics | - |
dc.subject.mesh | Cystic Fibrosis - complications - genetics | - |
dc.subject.mesh | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | - |
dc.subject.mesh | Mutation - genetics | - |
dc.subject.mesh | Vas Deferens - abnormalities | - |
dc.title | Identification of two mutations (S50Y and 4173delC) in the CFTR gene from patients with congenital bilateral absence of vas deferens (CBAVD) | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://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.email | Tsui, LC: tsuilc@hkucc.hku.hk | en_HK |
dc.identifier.authority | Tsui, LC=rp00058 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/(SICI)1098-1004(1997)9:2<183::AID-HUMU13>3.0.CO;2-Z | en_HK |
dc.identifier.pmid | 9067761 | - |
dc.identifier.scopus | eid_2-s2.0-0030950520 | en_HK |
dc.identifier.hkuros | 121044 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0030950520&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 9 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 183 | en_HK |
dc.identifier.epage | 184 | en_HK |
dc.identifier.isi | WOS:A1997WK78500013 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Zielenski, J=7003732699 | en_HK |
dc.identifier.scopusauthorid | Patrizio, P=7004465395 | en_HK |
dc.identifier.scopusauthorid | Markiewicz, D=7007146509 | en_HK |
dc.identifier.scopusauthorid | Asch, RH=35593760800 | en_HK |
dc.identifier.scopusauthorid | Tsui, LC=7102754167 | en_HK |
dc.identifier.issnl | 1059-7794 | - |