A small terminal deletion 11q in a boy without Jacobsen syndrome: Narrowing the critical region for the 11q Jacobsen syndrome phenotype

Abstract

American Journal of Medical Genetics Part AVolume 158A, Issue 3 p. 680-684 Research Letter A small terminal deletion 11q in a boy without Jacobsen syndrome: Narrowing the critical region for the 11q Jacobsen syndrome phenotype† Christina Evers, Corresponding Author Christina Evers christina.evers@med.uni-heidelberg.de Institute of Human Genetics, Heidelberg University, Heidelberg, GermanyInstitute of Human Genetics, Heidelberg University, Im Neuenheimer Feld 366, 69120 Heidelberg, Germany.Search for more papers by this authorJohannes W. G. Janssen, Johannes W. G. Janssen Institute of Human Genetics, Heidelberg University, Heidelberg, GermanySearch for more papers by this authorAnna Jauch, Anna Jauch Institute of Human Genetics, Heidelberg University, Heidelberg, GermanySearch for more papers by this authorMichael Bonin, Michael Bonin Medical Genetics Tübingen, Institute of Human Genetics, Tübingen, GermanySearch for more papers by this authorUte Moog, Ute Moog Institute of Human Genetics, Heidelberg University, Heidelberg, GermanySearch for more papers by this author Christina Evers, Corresponding Author Christina Evers christina.evers@med.uni-heidelberg.de Institute of Human Genetics, Heidelberg University, Heidelberg, GermanyInstitute of Human Genetics, Heidelberg University, Im Neuenheimer Feld 366, 69120 Heidelberg, Germany.Search for more papers by this authorJohannes W. G. Janssen, Johannes W. G. Janssen Institute of Human Genetics, Heidelberg University, Heidelberg, GermanySearch for more papers by this authorAnna Jauch, Anna Jauch Institute of Human Genetics, Heidelberg University, Heidelberg, GermanySearch for more papers by this authorMichael Bonin, Michael Bonin Medical Genetics Tübingen, Institute of Human Genetics, Tübingen, GermanySearch for more papers by this authorUte Moog, Ute Moog Institute of Human Genetics, Heidelberg University, Heidelberg, GermanySearch for more papers by this author First published: 02 February 2012 https://doi.org/10.1002/ajmg.a.34433Citations: 4 † How to Cite this Article: Evers C, Janssen JWG, Jauch A, Bonin M, Moog U. 2012. A small terminal deletion 11q in a boy without Jacobsen syndrome: Narrowing the critical region for the 11q Jacobsen syndrome phenotype. Am J Med Genet Part A 158A:680–684. Read the full textAboutPDF 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 onFacebookTwitterLinked InRedditWechat Citing Literature Volume158A, Issue3March 2012Pages 680-684 RelatedInformation