A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutations

Translated title of the contribution: A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutations

S. Vallette-Kasic, A.M. Pulichino, M. Gueydan, A. Barlier, M. David, G. Malpuech, C. Deal, G van Vliet, M. de Vroede, F. Riepe, C.J. Partsch, W. Sippell, M. Berberoglu, B. Atasay, F. Zegher, J. Kyllo, P. Donohoue, P. Dechelotte, M. Fassnacht, K. NoordamL. Dunkel, B. Pigeon, J. Weill, S. Yigit, R. Brauner, J. Leger, J.J. Heinrich, A. Enjalbert, T Brue, J. Drouin

Research output: Contribution to journalArticleAcademicpeer-review

Translated title of the contributionA neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutations
Original languageUndefined/Unknown
Pages (from-to)943-944
Number of pages2
JournalEndocrine research
Volume30
Issue number4
Publication statusPublished - 2004

Keywords

  • Econometric and Statistical Methods: General
  • Genetics
  • Geneeskunde(GENK)
  • Algemeen onderzoek
  • Internal medicine

Cite this