Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.

Auteurs

Vanbelleghem E, Van Damme T, Beyens A, Symoens S, Claes K, De Backer J, Meerschaut I, Vanommeslaeghe F, Delanghe SE, van den Ende J, Beyltjens T, Scimone ER, Lindsay ME, Schimmenti LA, Hinze AM, Dunn E, Gomez-Ospina N, Vandernoot I, Delguste T, Coppens S, Cormier-Daire V, Tartaglia M, Garavelli L, Shieh J, Demir Ş, Arslan Ateş E, Zenker M, Rohanizadegan M, Rivera-Cruz G, Douzgou S, Lin AE, Callewaert B

  • Date de publication

    July 2024
  • Type

    Article
  • Review

    Eur J Hum Genet
  • Researcher's name

    Coppens Sandra
  • Hôpital

    Hôpital Erasme
  • Service

    Génétique
  • PMID

    38997468
  • DOI

    10.1038/s41431-024-01664-1