A novel 22q11.2 microdeletion in DiGeorge syndrome.

Podobne zapisy

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