Clinical utility gene card for: DiGeorge syndrome, velocardiofacial syndrome, Shprintzen syndrome, chromosome 22q11.2 deletion syndrome (22q11.2, TBX1)

Lignende værker

• Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes
  af: Delio, Maria, et al.
  Udgivet: (2013)
• Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes
  af: Delio, Maria, et al.
  Udgivet: (2013)
• Secondary Immunologic Consequences in Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
  af: Zemble, R., et al.
  Udgivet: (2010)
• Independent De Novo 22q11.2 Deletions in First Cousins With DiGeorge/Velocardiofacial Syndrome
  af: Saitta, Sulagna C., et al.
  Udgivet: (2004)
• A novel 22q11.2 microdeletion in DiGeorge syndrome.
  af: Rauch, A, et al.
  Udgivet: (1999)