A novel 22q11.2 microdeletion in DiGeorge syndrome.

Ítems similars

• A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.
  per: Driscoll, D A, et al.
  Publicat: (1992)
• Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH
  per: Bittel, D.C., et al.
  Publicat: (2009)
• Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes
  per: Delio, Maria, et al.
  Publicat: (2013)
• Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes
  per: Delio, Maria, et al.
  Publicat: (2013)
• Clinical utility gene card for: DiGeorge syndrome, velocardiofacial syndrome, Shprintzen syndrome, chromosome 22q11.2 deletion syndrome (22q11.2, TBX1)
  per: Schwinger, Eberhard, et al.
  Publicat: (2010)