7q11.23-q21.2 Microdeletion is associated with moderate structural brain abnormalities and global developmental delay: first report

Ítems similars

• Identification of familial and de novo microduplications of 22q11.21–q11.23 distal to the 22q11.21 microdeletion syndrome region
  per: Coppinger, Justine, et al.
  Publicat: (2009)
• Implications of a Chr7q21.11 Microdeletion and the Role of the PCLO Gene in Developmental Delay
  per: Mazzaschi, Roberto L., et al.
  Publicat: (2013)
• Rare Case of a Heterozygous Microdeletion 9q21.11-q21.2: Clinical and Genetic Characteristics
  per: Ivanov, HY, et al.
  Publicat: (2018)
• Infantile Spasms Is Associated with Deletion of the MAGI2 Gene on Chromosome 7q11.23-q21.11
  per: Marshall, Christian R., et al.
  Publicat: (2008)
• Aripiprazole reversed gastroparesis in a child with 1q21.1–q21.2 microdeletion
  per: Rabinowitz, Simon S, et al.
  Publicat: (2018)