Abstract

American Journal of Medical Genetics Part AVolume 143A, Issue 4 p. 410-411 Correspondence Maternal serum screening and 22q11.2 deletion syndrome† Michael L. Begleiter, Corresponding Author Michael L. Begleiter [email protected] Section of Medical Genetics and Molecular Medicine, The Children's Mercy Hospitals and Clinics, Kansas City, Missouri The University of Missouri-Kansas City School of Medicine, Kansas City, MissouriSection of Medical Genetics and Molecular Medicine, The Children's Mercy Hospitals and Clinics, 2401 Gillham Road, Kansas City, MO 64108.Search for more papers by this authorMolly M. Lund, Molly M. Lund Section of Medical Genetics and Molecular Medicine, The Children's Mercy Hospitals and Clinics, Kansas City, Missouri The University of Missouri-Kansas City School of Medicine, Kansas City, MissouriSearch for more papers by this authorAndrea M. Atherton, Andrea M. Atherton Section of Medical Genetics and Molecular Medicine, The Children's Mercy Hospitals and Clinics, Kansas City, Missouri The University of Missouri-Kansas City School of Medicine, Kansas City, MissouriSearch for more papers by this authorJanda D. Buchholz, Janda D. Buchholz Section of Medical Genetics and Molecular Medicine, The Children's Mercy Hospitals and Clinics, Kansas City, Missouri The University of Missouri-Kansas City School of Medicine, Kansas City, MissouriSearch for more papers by this authorHolly H. Ardinger, Holly H. Ardinger Section of Medical Genetics and Molecular Medicine, The Children's Mercy Hospitals and Clinics, Kansas City, Missouri The University of Missouri-Kansas City School of Medicine, Kansas City, MissouriSearch for more papers by this author Michael L. Begleiter, Corresponding Author Michael L. Begleiter [email protected] Section of Medical Genetics and Molecular Medicine, The Children's Mercy Hospitals and Clinics, Kansas City, Missouri The University of Missouri-Kansas City School of Medicine, Kansas City, MissouriSection of Medical Genetics and Molecular Medicine, The Children's Mercy Hospitals and Clinics, 2401 Gillham Road, Kansas City, MO 64108.Search for more papers by this authorMolly M. Lund, Molly M. Lund Section of Medical Genetics and Molecular Medicine, The Children's Mercy Hospitals and Clinics, Kansas City, Missouri The University of Missouri-Kansas City School of Medicine, Kansas City, MissouriSearch for more papers by this authorAndrea M. Atherton, Andrea M. Atherton Section of Medical Genetics and Molecular Medicine, The Children's Mercy Hospitals and Clinics, Kansas City, Missouri The University of Missouri-Kansas City School of Medicine, Kansas City, MissouriSearch for more papers by this authorJanda D. Buchholz, Janda D. Buchholz Section of Medical Genetics and Molecular Medicine, The Children's Mercy Hospitals and Clinics, Kansas City, Missouri The University of Missouri-Kansas City School of Medicine, Kansas City, MissouriSearch for more papers by this authorHolly H. Ardinger, Holly H. Ardinger Section of Medical Genetics and Molecular Medicine, The Children's Mercy Hospitals and Clinics, Kansas City, Missouri The University of Missouri-Kansas City School of Medicine, Kansas City, MissouriSearch for more papers by this author First published: 17 January 2007 https://doi.org/10.1002/ajmg.a.31616Citations: 5 † How to cite this article: Begleiter ML, Lund MM, Atherton AM, Buchholz JD, Ardinger HH. 2007. Maternal serum screening and 22q11.2 deletion syndrome. Am J Med Genet Part A. 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 No abstract is available for this article.Citing Literature Volume143A, Issue415 February 2007Pages 410-411 RelatedInformation

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