Clinical Report

Diagnosis of a terminal deletion of 4p with duplication of Xp22.31 in a patient with findings of Opitz G/BBB syndrome and Wolf–Hirschhorn syndrome†

  1. Joyce So1,
  2. Ines Müller1,
  3. Melanie Kunath1,
  4. Susanne Herrmann2,
  5. Reinhard Ullmann1,*,
  6. Susann Schweiger1,3

Article first published online: 11 DEC 2007

DOI: 10.1002/ajmg.a.32055

Issue

American Journal of Medical Genetics Part A

American Journal of Medical Genetics Part A

Volume 146A, Issue 1, pages 103–109, 1 January 2008

Additional Information

How to Cite

So, J., Müller, I., Kunath, M., Herrmann, S., Ullmann, R. and Schweiger, S. (2008), Diagnosis of a terminal deletion of 4p with duplication of Xp22.31 in a patient with findings of Opitz G/BBB syndrome and Wolf–Hirschhorn syndrome. Am. J. Med. Genet., 146A: 103–109. doi: 10.1002/ajmg.a.32055

Author Information

  1. 1

    Max Planck Institute for Molecular Genetics, Berlin, Germany

  2. 2

    Children's Hospital, Friedrich Schiller University, Jena, Germany

  3. 3

    Charité Hospital, Department of Dermatology, Berlin, Germany

*Max Planck Institute for Molecular Genetics, Ihnestr. 73, 14195 Berlin, Germany.

  1. †

    How to cite this article: So J, Müller I, Kunath M, Herrmann S, Ullmann R, Schweiger S. 2007. Diagnosis of a terminal deletion of 4p with duplication of Xp22.31 in a patient with findings of Opitz G/BBB syndrome and Wolf–Hirschhorn syndrome. Am J Med Genet Part A 146A:103–109.

Publication History

  1. Issue published online: 19 DEC 2007
  2. Article first published online: 11 DEC 2007
  3. Manuscript Accepted: 11 JUL 2007
  4. Manuscript Received: 27 APR 2007

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