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

Slični predmeti

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