A Case of 17q21.31 Microduplication and 7q31.33 Microdeletion, Associated with Developmental Delay, Microcephaly, and Mild Dysmorphic Features

Những quyển sách tương tự

• Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition.
  Bằng: Thomas Arbogast, et al.
  Được phát hành: (2017-07-01)
• Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition
  Bằng: Arbogast, Thomas, et al.
  Được phát hành: (2017)
• Complex Phenotype Associated with 17q21.31 Microdeletion
  Bằng: Dornelles-Wawruk, H., et al.
  Được phát hành: (2013)
• 7q35 Microdeletion and 15q13.3 and Xp22.33 Microduplications in a Patient with Severe Myoclonic Epilepsy, Microcephaly, Dysmorphisms, Severe Psychomotor Delay and Intellectual Disability
  Bằng: Paduano, Francesco, et al.
  Được phát hành: (2020)
• Clinical and molecular delineation of the 17q21.31 microdeletion syndrome
  Bằng: Koolen, D A, et al.
  Được phát hành: (2008)