De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes

Antzeko izenburuak

• Two further cases of WHS with unbalanced de novo translocation t(4;8) characterised by CGH and FISH
  nork: Tonnies, H., et al.
  Argitaratua: (2001)
• Fluorescent in situ hybridisation (FISH) for hemizygous deletion at the elastin locus in patients with isolated supravalvular aortic stenosis.
  nork: Fryssira, H, et al.
  Argitaratua: (1997)
• GE-26 ASSOCIATION BETWEEN FLUORESCENCE IN SITU HYBRIDISATION (FISH) PROBE RATIO SCORES AND SURVIVAL IN 1p/19q CO-DELETED GLIOMAS
  nork: Pinkham, Mark, et al.
  Argitaratua: (2014)
• Measurement of locus copy number by hybridisation with amplifiable probes
  nork: Armour, John A. L., et al.
  Argitaratua: (2000)
• NF1 Microdeletion Syndrome: Refined FISH Characterization of Sporadic and Familial Deletions with Locus-Specific Probes
  nork: Riva, Paola, et al.
  Argitaratua: (2000)