Deletions of Xp Provide Evidence for the Role of Holocytochrome C-Type Synthase (HCCS) in Congenital Diaphragmatic Hernia

Ítems similars

• Biosynthesis of single thioether c-type cytochromes provide insight into mechanisms intrinsic to holocytochrome c synthase (HCCS)
  per: Babbitt, Shalon E., et al.
  Publicat: (2017)
• Genetic aspects of human congenital diaphragmatic hernia
  per: Pober, BR
  Publicat: (2008)
• Intragenic deletions of the IGF1 receptor gene in five individuals with psychiatric phenotypes and developmental delay
  per: Witsch, Jens, et al.
  Publicat: (2013)
• Chromosome 8p23.1 Deletions as a Cause of Complex Congenital Heart Defects and Diaphragmatic Hernia
  per: Wat, Margaret J., et al.
  Publicat: (2009)
• DIAPHRAGMATIC HERNIA
  per: Dickson, W. H.
  Publicat: (1933)