Deletion 16p13.11 uncovers <i>NDE1</i> mutations on the non‐deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption

Ítems similars

• Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption
  per: Paciorkowski, Alex R, et al.
  Publicat: (2013)
• Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review
  per: Tan, Li, et al.
  Publicat: (2017)
• A rare 19p13.11-p13.12 deletion in a patient with microcephaly and developmental delay
  per: Laiara Cristina de Souza, et al.
  Publicat: (2018)
• Neuropathology of 16p13.11 Deletion in Epilepsy
  per: Liu, Joan Y. W., et al.
  Publicat: (2012)
• Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly
  per: Alkuraya, Fowzan S., et al.
  Publicat: (2011)