Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant

Míreanna comhchosúla

• Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.
  de réir: Hannes, F, et al.
  Foilsithe / Cruthaithe: (2009)
• Establishment of induced pluripotent stem cells from a patient with 16p13.11 duplication and VPS13B deletion
  de réir: Hiroki Okumura, et al.
  Foilsithe / Cruthaithe: (2022-10-01)
• Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series
  de réir: Martina Busè, et al.
  Foilsithe / Cruthaithe: (2017-07-01)
• Codes correcting bursts of deletions/insertions and tandem duplications
  de réir: Nguyen, Tuan Thanh
  Foilsithe / Cruthaithe: (2018)
• Chimeric Genes in Deletions and Duplications Associated with Intellectual Disability
  de réir: Sonia Mayo, et al.
  Foilsithe / Cruthaithe: (2017-01-01)