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Recommendations for standardized human pedigree nomenclature

dc.contributor.authorSteinhaus, Kathryn A.en_US
dc.contributor.authorO'Sullivan, Corrine K.en_US
dc.contributor.authorHamanishi, Janen_US
dc.contributor.authorVincent, Victoriaen_US
dc.contributor.authorMarkel, Dorene S.en_US
dc.contributor.authorLochner-Doyle, Debraen_US
dc.contributor.authorBennett, Robin L.en_US
dc.contributor.authorUhrich, Stefanie B.en_US
dc.contributor.authorResta, Robert G.en_US
dc.date.accessioned2006-09-11T15:27:10Z
dc.date.available2006-09-11T15:27:10Z
dc.date.issued1995-12en_US
dc.identifier.citationBennett, Robin L.; Steinhaus, Kathryn A.; Uhrich, Stefanie B.; O'Sullivan, Corrine K.; Resta, Robert G.; Lochner-Doyle, Debra; Markel, Dorene S.; Vincent, Victoria; Hamanishi, Jan; (1995). "Recommendations for standardized human pedigree nomenclature." Journal of Genetic Counseling 4(4): 267-279. <http://hdl.handle.net/2027.42/44926>en_US
dc.identifier.issn1573-3599en_US
dc.identifier.issn1059-7700en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44926
dc.description.abstractThe construction of an accurate family pedigree is a fundamental component of a clinical genetic evaluation and of human genetic research. Previous surveys of genetic counselors and human genetic publications have demonstrated significant inconsistencies in the usage of common pedigree symbols representing situations such as pregnancy, termination of pregnancy, miscarriage, and adoption, as well as less common scenarios such as pregnancies conceived through assisted reproductive technologies. The Pedigree Standardization Task Force (PSTF) was organized through the Professional Issues Committee of the National Society of Genetic Counselors, to establish recommendations for universal standards in human pedigree nomenclature. Nomenclature was chosen based on current usage, consistency among symbols, computer compatibility, and the adaptability of symbols to reflect the rapid technical advances in human genetics. Preliminary recommendations were presented for review at three national meetings of human genetic professionals and sent to >100 human genetic professionals for review. On the basis of this review process, the recommendations of the PSTF for standardized human pedigree nomenclature are presented here. By incorporating these recommendations into medical genetics professional training programs, board examinations, genetic publications, and pedigree software, the adoption of uniform pedigree nomenclature can begin. Usage of standardized pedigree nomenclature will reduce the chances for incorrect interpretation of patient and family medical and genetic information. It may also improve the quality of patient care provided by genetic professionals and facilitate communication between researchers involved with genetic family studies.en_US
dc.format.extent819730 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers-Human Sciences Press; National Society of Genetic Counselors, Inc. ; Springer Science+Business Mediaen_US
dc.subject.otherHuman Geneticsen_US
dc.subject.otherGynecologyen_US
dc.subject.otherClinical Psychologyen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherEthicsen_US
dc.subject.otherPublic Health/Gesundheitswesenen_US
dc.titleRecommendations for standardized human pedigree nomenclatureen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumHuman Genome Center, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherCenter for Perinatal Studies, Swedish Medical Center, Seattle, Washingtonen_US
dc.contributor.affiliationotherGenetics Services Section, Department of Health, Seattle, Washingtonen_US
dc.contributor.affiliationotherDivision of Medical Genetics, University of Washington Medical Center, Seattle, Washington; Medical Genetics, RG-25, University of Washington Medical Center, 98195, Seattle, Washingtonen_US
dc.contributor.affiliationotherDivision of Human Genetics, University of California at Irvine, Orange, Californiaen_US
dc.contributor.affiliationotherObstetrics and Gynecology, University of Washington Medical Center, Seattle, Washingtonen_US
dc.contributor.affiliationotherMedical Genetics, RG-25, University of Washington Medical Center, 98195, Seattle, Washingtonen_US
dc.contributor.affiliationotherDivision of Genetics, University of South Carolina School of Medicine, Columbia, South Carolinaen_US
dc.contributor.affiliationotherObstetrics and Gynecology, University of Washington Medical Center, Seattle, Washingtonen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid24234481en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44926/1/10897_2005_Article_BF01408073.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF01408073en_US
dc.identifier.sourceJournal of Genetic Counselingen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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