Next generation diagnostics on cardiomyopathy

Lignende værker

• CATCHing putative causative variants in consanguineous families
  af: Santoni, Federico Andrea, et al.
  Udgivet: (2015)
• Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster
  af: Santoni, Federico A., et al.
  Udgivet: (2014)
• Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree
  af: Makrythanasis, Periklis, et al.
  Udgivet: (2016)
• TNPO3 protects HIV-1 replication from CPSF6-mediated capsid stabilization in the host cell cytoplasm
  af: De Iaco, Alberto, et al.
  Udgivet: (2013)
• From sequence to functional understanding: the difficult road ahead
  af: Makrythanasis, Periklis, et al.
  Udgivet: (2011)