Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: case report

Eitemau Tebyg

• Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: case report
  gan: Bejjani Bassem A, et al.
  Cyhoeddwyd: (2009-01-01)
• Infantile spasms related to a 5q31.2-q31.3 microdeletion including PURA
  gan: Shimojima, Keiko, et al.
  Cyhoeddwyd: (2018)
• Long-term follow-up of a patient with 5q31.3 microdeletion syndrome and the smallest de novo 5q31.2q31.3 deletion involving PURA
  gan: Bonaglia, Maria Clara, et al.
  Cyhoeddwyd: (2015)
• A novel insertion ins(18;5)(q21.1;q31.2q35.1) in acute myeloid leukemia associated with microdeletions at 5q31.2, 5q35.1q35.2 and 18q12.3q21.1 detected by oligobased array comparative genomic hybridization
  gan: Kjeldsen, Eigil
  Cyhoeddwyd: (2014)
• Duplication at chromosome 2q31.1-q31.2 in a family presenting syndactyly and nystagmus
  gan: Ghoumid, Jamal, et al.
  Cyhoeddwyd: (2011)