Detection of an Atypical 22q11 Deletion That Has No Overlap with the DiGeorge Syndrome Critical Region

This publication has 17 references indexed in Scilit:

• A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11
  Human Molecular Genetics, 1996
• Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome
  Human Molecular Genetics, 1995
• Autosomal dominant “Opitz” GBBB syndrome due to a 22q11. 2 deletion
  American Journal of Medical Genetics, 1995
• Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene
  Nature Genetics, 1995
• Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome
  Human Molecular Genetics, 1995
• Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity
  Human Molecular Genetics, 1995
• Deletions and microdeletions of 22q11.2 in velo‐cardio‐facial syndrome
  American Journal of Medical Genetics, 1992
• Deletions within chromosome 22q11 in familial congenital heart disease
  The Lancet, 1992
• Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus
  The Lancet, 1992
• Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome
  Genomics, 1991