Differential allelic expression of a fibrillin gene (FBN1) in patients with Marfan syndrome.

Những quyển sách tương tự

• A new missense mutation of fibrillin in a patient with Marfan syndrome.
  Bằng: Hewett, D R, et al.
  Được phát hành: (1994)
• Analyses of truncated fibrillin caused by a 366 bp deletion in the FBN1 gene resulting in Marfan syndrome.
  Bằng: Raghunath, M, et al.
  Được phát hành: (1994)
• Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndrome.
  Bằng: Wang, M, et al.
  Được phát hành: (1996)
• Characterisation of four novel fibrillin-1 (FBN1) mutations in Marfan syndrome.
  Bằng: Adès, L C, et al.
  Được phát hành: (1996)
• AB150. Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome
  Bằng: Hsieh, Shu-Chen, et al.
  Được phát hành: (2015)