22Q11 - PHYSICAL, COMPARATIVE AND DISEASE LOCUS MAPPING

Antzeko izenburuak

• Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease.
  nork: Halford, S, et al.
  Argitaratua: (1993)
• MOLECULAR STUDIES OF MONOSOMY-22Q11 AND ITS CLINICAL CONSEQUENCES
  nork: Scambler, P, et al.
  Argitaratua: (1991)
• Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11.
  nork: Halford, S, et al.
  Argitaratua: (1993)
• CATCH-22 - CAN MOLECULAR GENETICS EXPLAIN THE PHENOTYPE
  nork: Halford, S, et al.
  Argitaratua: (1995)
• A novel C2H2 zinc-finger protein gene (ZNF160) maps to human chromosome 19q13.3-q13.4.
  nork: Halford, S, et al.
  Argitaratua: (1995)