Rubinstein-Taybi syndrome with deletions of FISH probe RT1 at 16p13.3: two UK patients.

Ítems similars

• Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3
  per: Breuning, Martijn H., et al.
  Publicat: (1993)
• Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome: clinical aspects.
  per: Hennekam, R C, et al.
  Publicat: (1993)
• Medical genetics: advances in brief: Rubinstein-Taybi syndrome caused by submicroscopic deletions with 16p13.3
  per: Goodship, Judith
  Publicat: (1993)
• Submicroscopic deletions at 16p13.3 in Rubinstein-Taybi syndrome: frequency and clinical manifestations in a North American population.
  per: Wallerstein, R, et al.
  Publicat: (1997)
• Rubinstein-Taybi syndrome.
  per: Berry, A C
  Publicat: (1987)