MOLECULAR STUDIES OF MONOSOMY-22Q11 AND ITS CLINICAL CONSEQUENCES

Míreanna comhchosúla

• Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome.
  de réir: Carey, A, et al.
  Foilsithe / Cruthaithe: (1992)
• 22Q11 - PHYSICAL, COMPARATIVE AND DISEASE LOCUS MAPPING
  de réir: Halford, S, et al.
  Foilsithe / Cruthaithe: (1994)
• Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome.
  de réir: Halford, S, et al.
  Foilsithe / Cruthaithe: (1993)
• Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134).
  de réir: Wadey, R, et al.
  Foilsithe / Cruthaithe: (1993)
• Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11.
  de réir: Halford, S, et al.
  Foilsithe / Cruthaithe: (1993)