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

समान संसाधन

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