Germline mutation in DOK7 associated with fetal akinesia deformation sequence.

Lignende værker

• Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patients.
  af: Vogt, J, et al.
  Udgivet: (2008)
• Mutation analysis of CHRNA1, CHRNB1, CHRND and RAPSN genes in multiple pterygium syndrome/fetal akinesia patients
  af: Vogt, J, et al.
  Udgivet: (2007)
• Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence.
  af: Edith Bonnin, et al.
  Udgivet: (2018-12-01)
• Alteration of actin cytoskeletal organisation in fetal akinesia deformation sequence
  af: Ramona Jühlen, et al.
  Udgivet: (2024-01-01)
• Identification of four TTN variants in three families with fetal akinesia deformation sequence
  af: Lihong Fan, et al.
  Udgivet: (2024-06-01)