Co-occurrence of 16p13.11 microdeletion and ring chromosome 20 syndrome

समान संसाधन

• Clinical utility gene card for: 16p13.11 microdeletion syndrome
  द्वारा: Tropeano, Maria, और अन्य
  प्रकाशित: (2014)
• Phenotypic manifestations of copy number variation in chromosome 16p13.11
  द्वारा: Nagamani, Sandesh C Sreenath, और अन्य
  प्रकाशित: (2011)
• Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
  द्वारा: de Kovel, Carolien G. F., और अन्य
  प्रकाशित: (2010)
• Neuropathology of 16p13.11 Deletion in Epilepsy
  द्वारा: Liu, Joan Y. W., और अन्य
  प्रकाशित: (2012)
• Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review
  द्वारा: Tan, Li, और अन्य
  प्रकाशित: (2017)