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Article: Genotype and phenotype in cystic fibrosis

TitleGenotype and phenotype in cystic fibrosis
Authors
Tsui, LCDurie, P
Issue Date1997
PublisherMcGraw-Hill Companies, Inc. The Journal's web site is located at http://www.hosppract.com
Citation
Hospital Practice, 1997, v. 32 n. 6, p. 115-118+123-129+134+140+142 How to Cite?
DOI: http://dx.doi.org/10.1080/21548331.1997.11443512
AbstractQuestions about the function of the disease-related gene are still not fully answered, but correlations are emerging between specific mutations and a patient's clinical condition. The strongest link is for pancreatic failure. A second involves azoospermia. Indeed, mutations are being found in males with infertility as the sole sign of disease. Improved knowledge of such patterns may suggest novel approaches to severe cystic fibrosis.
Persistent Identifierhttp://hdl.handle.net/10722/143121
ISSN
8750-2836
ISI Accession Number ID
WOS:A1997XE19300012
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorTsui, LCen_HK
dc.contributor.authorDurie, Pen_HK
dc.date.accessioned2011-11-01T08:35:05Z-
dc.date.available2011-11-01T08:35:05Z-
dc.date.issued1997en_HK
dc.identifier.citationHospital Practice, 1997, v. 32 n. 6, p. 115-118+123-129+134+140+142en_HK
dc.identifier.issn8750-2836en_HK
dc.identifier.urihttp://hdl.handle.net/10722/143121-
dc.description.abstractQuestions about the function of the disease-related gene are still not fully answered, but correlations are emerging between specific mutations and a patient's clinical condition. The strongest link is for pancreatic failure. A second involves azoospermia. Indeed, mutations are being found in males with infertility as the sole sign of disease. Improved knowledge of such patterns may suggest novel approaches to severe cystic fibrosis.en_HK
dc.languageeng-
dc.publisherMcGraw-Hill Companies, Inc. The Journal's web site is located at http://www.hosppract.com-
dc.relation.ispartofHospital Practiceen_HK
dc.subject.meshBlood Proteins - genetics - physiology-
dc.subject.meshCystic Fibrosis - genetics-
dc.subject.meshCystic Fibrosis Transmembrane Conductance Regulator - genetics - physiology-
dc.subject.meshGenotype-
dc.subject.meshPhenotype-
dc.titleGenotype and phenotype in cystic fibrosisen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=2154-8331&volume=32&issue=6&spage=115&epage=118, 123&date=1997&atitle=Genotype+and+phenotype+in+cystic+fibrosis-
dc.identifier.emailTsui, LC: tsuilc@hkucc.hku.hken_HK
dc.identifier.authorityTsui, LC=rp00058en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1080/21548331.1997.11443512-
dc.identifier.pmid9194805-
dc.identifier.scopuseid_2-s2.0-1842333889en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-1842333889&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume32en_HK
dc.identifier.issue6en_HK
dc.identifier.spage115en_HK
dc.identifier.epage118+123en_HK
dc.identifier.isiWOS:A1997XE19300012-
dc.identifier.scopusauthoridTsui, LC=7102754167en_HK
dc.identifier.scopusauthoridDurie, P=7005360997en_HK
dc.identifier.issnl8750-2836-

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