Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome

Những quyển sách tương tự

• Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22–q24.1
  Bằng: Ishihara, N, et al.
  Được phát hành: (2004)
• Systematic assessment of atypical deletions reveals genotype–phenotype correlation in 22q11.2
  Bằng: Rauch, A, et al.
  Được phát hành: (2005)
• Neurological Phenotype of Mowat-Wilson Syndrome
  Bằng: Cordelli, Duccio Maria, et al.
  Được phát hành: (2021)
• Mowat–Wilson syndrome and mutation in the zinc finger homeo box 1B gene: a well defined clinical entity
  Bằng: Cerruti, M, et al.
  Được phát hành: (2004)
• Clinical utility gene card for: Mowat–Wilson syndrome
  Bằng: Zollino, Marcella, et al.
  Được phát hành: (2011)