Publications

• Expanding the phenotypic spectrum of ARCN1-related syndrome.
  Genet Med Volume: 24 Page(s): 1227 - 1237
  06/01/2022 Authors: Ritter AL; Gold J; Hayashi H; Ackermann AM; Hanke S; Skraban C; Cuddapah S; Bhoj E; Li D; Kuroda Y
• A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
  J Med Genet Volume: 49 Page(s): 660 - 668
  10/01/2012 Authors: Zufferey F; Sherr EH; Beckmann ND; Hanson E; Maillard AM; Hippolyte L; Mac A; Ferrari C; Kutalik Z; Andrieux J