Specific Association of Missense Mutations in CRELD1 with Cardiac Atrioventricular Septal Defects in Heterotaxy Syndrome

Ítems similars

• Missense Mutations in CRELD1 Are Associated with Cardiac Atrioventricular Septal Defects
  per: Robinson, Susan W., et al.
  Publicat: (2003)
• Allelic Interaction between CRELD1 and VEGFA in the Pathogenesis of Cardiac Atrioventricular Septal Defects
  per: Redig, Jennifer K., et al.
  Publicat: (2014)
• Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms
  per: Burnicka-Turek, Ozanna, et al.
  Publicat: (2016)
• Missense mutation G296S in GATA4 is not responsible for cardiac septal defects
  per: Ramegowda, Smitha, et al.
  Publicat: (2007)
• Contribution of Copy Number Variation to Down Syndrome-associated Atrioventricular Septal Defects
  per: Ramachandran, Dhanya, et al.
  Publicat: (2014)