Clinical Report

New case of interstitial deletion 12(q15-q21.2) in a girl with facial dysmorphism and mental retardation†

  1. Caroline Schluth1,
  2. Roselyne Gesny2,
  3. Guntram Borck2,
  4. Richard Redon3,
  5. Véronique Abadie4,
  6. Pascale Kleinfinger5,
  7. Arnold Munnich1,
  8. Stanislas Lyonnet1,*,
  9. Laurence Colleaux2

Article first published online: 11 DEC 2007

DOI: 10.1002/ajmg.a.31869

Issue

American Journal of Medical Genetics Part A

American Journal of Medical Genetics Part A

Volume 146A, Issue 1, pages 93–96, 1 January 2008

Additional Information

How to Cite

Schluth, C., Gesny, R., Borck, G., Redon, R., Abadie, V., Kleinfinger, P., Munnich, A., Lyonnet, S. and Colleaux, L. (2008), New case of interstitial deletion 12(q15-q21.2) in a girl with facial dysmorphism and mental retardation. Am. J. Med. Genet., 146A: 93–96. doi: 10.1002/ajmg.a.31869

Author Information

  1. 1

    Département de Génétique, Hôpital Necker Enfants Malades, Paris, France

  2. 2

    INSERM U781, Universite Paris V, Paris, France

  3. 3

    The Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK

  4. 4

    Service de Pédiatrie Générale, Hôpital Necker Enfants Malades, Paris, France

  5. 5

    Laboratoire Pasteur-Cerba, Saint Ouen L'Aumone, France

*Service de Génétique Médicale, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75753 Paris Cedex 15, France.

  1. †

    How to cite this article: Schluth C, Gesny R, Borck G, Redon R, Abadie V, Kleinfinger P, Munnich A, Lyonnet S, Colleaux L. 2007. New case of interstitial deletion 12(q15-q21.2) in a girl with facial dysmorphism and mental retardation. Am J Med Genet Part A 146A:93–96.

Publication History

  1. Issue published online: 19 DEC 2007
  2. Article first published online: 11 DEC 2007
  3. Manuscript Accepted: 22 APR 2007
  4. Manuscript Received: 7 JUN 2006

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