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

Podobne zapisy

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