De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism

  • Illja J Diets
  • , Roos van der Donk
  • , Kristina Baltrunaite
  • , Esmé Waanders
  • , Margot R F Reijnders
  • , Alexander J M Dingemans
  • , Rolph Pfundt
  • , Anneke T Vulto-van Silfhout
  • , Laurens Wiel
  • , Christian Gilissen
  • , Julien Thevenon
  • , Laurence Perrin
  • , Alexandra Afenjar
  • , Caroline Nava
  • , Boris Keren
  • , Sarah Bartz
  • , Bethany Peri
  • , Gea Beunders
  • , Nienke Verbeek
  • , Koen van Gassen
    • Isabelle Thiffault, Maxime Cadieux-Dion, Lina Huerta-Saenz, Matias Wagner, Vassiliki Konstantopoulou, Julia Vodopiutz, Matthias Griese, Annekatrien Boel, Bert Callewaert, Han G Brunner, Tjitske Kleefstra, Nicoline Hoogerbrugge, Bert B A de Vries, Vivian Hwa, Andrew Dauber, Jayne Y Hehir-Kwa, Roland Kuiper, Marjolijn Jongmans

Research output: Contribution to journal › Article › peer-review

40 Citations (Scopus)

Fingerprint

Dive into the research topics of 'De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism'. Together they form a unique fingerprint.
Sort by

Keyphrases

Biochemistry, Genetics and Molecular Biology