Abstract: Prenatal DiagnosisVolume 30, Issue 2 p. 173-176 Research LetterFull Access Double trisomy revisited—a multicenter experience Mark Micale, Corresponding Author Mark Micale [email protected] Department of Anatomic Pathology, William Beaumont Hospital, Royal Oak, MI, USA Oakland University William Beaumont School of Medicine, Rochester, MI, USADepartment of Anatomic Pathology, William Beaumont Hospital, 3601 W. Thirteen Mile Rd, Royal Oak, MI 48073-6769, USA.Search for more papers by this authorJanet Insko, Janet Insko Department of Anatomic Pathology, William Beaumont Hospital, Royal Oak, MI, USASearch for more papers by this authorSalah A. D. Ebrahim, Salah A. D. Ebrahim DMC University Laboratories and Wayne State University School of Medicine, Detroit, MI, USASearch for more papers by this authorAdewale Adeyinka, Adewale Adeyinka Department of Medical Genetics, Henry Ford Hospital, Detroit, MI, USASearch for more papers by this authorCassandra Runke, Cassandra Runke Department of Pathology and Laboratory Medicine, Mayo Clinic, Rochester, MN, USASearch for more papers by this authorDaniel L. Van Dyke, Daniel L. Van Dyke Department of Pathology and Laboratory Medicine, Mayo Clinic, Rochester, MN, USASearch for more papers by this author Mark Micale, Corresponding Author Mark Micale [email protected] Department of Anatomic Pathology, William Beaumont Hospital, Royal Oak, MI, USA Oakland University William Beaumont School of Medicine, Rochester, MI, USADepartment of Anatomic Pathology, William Beaumont Hospital, 3601 W. Thirteen Mile Rd, Royal Oak, MI 48073-6769, USA.Search for more papers by this authorJanet Insko, Janet Insko Department of Anatomic Pathology, William Beaumont Hospital, Royal Oak, MI, USASearch for more papers by this authorSalah A. D. Ebrahim, Salah A. D. Ebrahim DMC University Laboratories and Wayne State University School of Medicine, Detroit, MI, USASearch for more papers by this authorAdewale Adeyinka, Adewale Adeyinka Department of Medical Genetics, Henry Ford Hospital, Detroit, MI, USASearch for more papers by this authorCassandra Runke, Cassandra Runke Department of Pathology and Laboratory Medicine, Mayo Clinic, Rochester, MN, USASearch for more papers by this authorDaniel L. Van Dyke, Daniel L. Van Dyke Department of Pathology and Laboratory Medicine, Mayo Clinic, Rochester, MN, USASearch for more papers by this author First published: 29 December 2009 https://doi.org/10.1002/pd.2429Citations: 16AboutPDF 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 onEmailFacebookTwitterLinkedInRedditWechat REFERENCES Altug-Teber O, Bonin M, Walter M, et al. 2007. Specific transcriptional changes in human fetuses with autosomal trisomies. Cytogenet Genome Res 119: 171–184. Benkhalifa M, Kasakyan S, Clement P, et al. 2005. 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