NKX2-5 molecular screening and assessment of variant rate and risk factors of secundum atrial septal defect in a Moroccan population

Lignende værker

• Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects
  af: El Bouchikhi, Ihssane, et al.
  Udgivet: (2020)
• GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot
  af: EL Bouchikhi, Ihssane, et al.
  Udgivet: (2018)
• Noonan syndrome-causing genes: Molecular update and an assessment of the mutation rate
  af: El Bouchikhi, Ihssane, et al.
  Udgivet: (2016)
• Molecular and presymptomatic analysis of a Moroccan Lynch syndrome family revealed a novel frameshift MLH1 germline mutation
  af: Moufid, Fatima Zahra, et al.
  Udgivet: (2018)
• The detection of a novel insertion mutation in exon 2 of the MEFV gene associated with familial mediterranean fever in a moroccan family
  af: Mejtoute, Touhami, et al.
  Udgivet: (2017)