Letter to the Editor

Potential for the prenatal diagnosis of hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome

  1. B. Chadefaux1,
  2. J. P. Bonnefont2,
  3. D. Rabier1,
  4. VE. Shih3,
  5. J. M. Saudubray2,
  6. P. Kamoun1,
  7. Giovanni Neri Editor,
  8. James F. Reynold Editor

Article first published online: 5 JUN 2005

DOI: 10.1002/ajmg.1320320228

Issue

American Journal of Medical Genetics

American Journal of Medical Genetics

Volume 32, Issue 2, page 264, February 1989

Additional Information

How to Cite

Chadefaux, B., Bonnefont, J. P., Rabier, D., Shih, VE., Saudubray, J. M., Kamoun, P., Neri, G. and Reynold, J. F. (1989), Potential for the prenatal diagnosis of hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome. Am. J. Med. Genet., 32: 264. doi: 10.1002/ajmg.1320320228

Author Information

  1. 1

    Laboratoire de Biochimie Médicale, B Massachusetts Hospital Boston

  2. 2

    Clinique de Génétique Médicale, Département de Pédiatrie Massachusetts Hospital Boston

  3. 3

    Hôpital Necker-Enfants Malades, Paris, France; Amino Acid Disorder Laboratory, Neurology Service Massachusetts Hospital Boston

Publication History

  1. Issue published online: 5 JUN 2005
  2. Article first published online: 5 JUN 2005
  3. Manuscript Revised: 15 JUL 1988
  4. Manuscript Received: 22 FEB 1988

Funded by

  • Association Française pour le Dépistage et la Prévention des Maladies Métaboliques et des Handicaps chez l'Enfant

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