Confirmation of the chromosome 8p23.1 euchromatic duplication as a variant with no clinical manifestations

Abstract

Prenatal DiagnosisVolume 19, Issue 2 p. 183-184 Letter to the EditorFree Access Confirmation of the chromosome 8p23.1 euchromatic duplication as a variant with no clinical manifestations D. P. O'Malley, Corresponding Author D. P. O'Malley Cytogenetics Laboratory, Michigan State University, B-120 Life Sciences Bldg, East Lansing, MI 48824, U.S.A.Manager, Cytogenetics Laboratory, Michigan State University, B-120 Life Sciences Bldg, East Lansing, MI 48824, U.S.A.Search for more papers by this authorP. D. Storto, P. D. Storto Cytogenetics Laboratory, Michigan State University, B-120 Life Sciences Bldg, East Lansing, MI 48824, U.S.A.Search for more papers by this author D. P. O'Malley, Corresponding Author D. P. O'Malley Cytogenetics Laboratory, Michigan State University, B-120 Life Sciences Bldg, East Lansing, MI 48824, U.S.A.Manager, Cytogenetics Laboratory, Michigan State University, B-120 Life Sciences Bldg, East Lansing, MI 48824, U.S.A.Search for more papers by this authorP. D. Storto, P. D. Storto Cytogenetics Laboratory, Michigan State University, B-120 Life Sciences Bldg, East Lansing, MI 48824, U.S.A.Search for more papers by this author First published: 14 April 1999 https://doi.org/10.1002/(SICI)1097-0223(199902)19:2<183::AID-PD481>3.0.CO;2-9Citations: 9AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES Barber, J.C.K., Joyce, C.A., Collinson, M.N., Nicholson, J.C., Willatt, L.R., Dyson, H.M., Bateman, M.S., Green, A.J., Yates, J.R.W., Dennis, R.D. (1998). Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance, J. Med. Genet., 35, 491– 496.Medline Joyce, C., Collinson, M., Barber, J. (1996). Validation of a subtelomeric probe and its amplification in cytogenetic duplications of 8p with no detectable phenotypic effect, J. Med. Genet., 33, A3.014. Williams, L., Larkins, S., Roberts, E., Davidson, E.V. (1996). Two further cases of variation in band 8p23.1. Not always a benign variant?, J. Med. Genet., 33, A3.020. Citing Literature Volume19, Issue2February 1999Pages 183-184 ReferencesRelatedInformation