A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome.

Samankaltaisia teoksia

• A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
  Tekijä: Fenwick, A, et al.
  Julkaistu: (2011)
• A deletion of <it>FGFR2 </it>creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
  Tekijä: Klatt Regan EM, et al.
  Julkaistu: (2011-09-01)
• Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily.
  Tekijä: Bochukova, E, et al.
  Julkaistu: (2009)
• Expression analysis of an FGFR2 IIIc 5' splice site mutation (1084+3A-&gt;G).
  Tekijä: Kan, R, et al.
  Julkaistu: (2004)
• Lunate excision with capitohamate fusion in the treatment of stage IIIB and IIIC Kienböck's disease
  Tekijä: Mesut Tahta, et al.
  Julkaistu: (2018-05-01)