Autosomal dominant congenital Horner's syndrome in a Dutch family.

مواد مشابهة

• A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family.
  بواسطة: Verzijl, H T, وآخرون
  منشور في: (1999)
• Autosomal dominant inheritance of Gerhardt's syndrome in three generations of a family.
  بواسطة: Morelli, G, وآخرون
  منشور في: (1980)
• The "harlequin" sign and congenital Horner's syndrome.
  بواسطة: Morrison, D A, وآخرون
  منشور في: (1997)
• Autosomal dominant burning feet syndrome
  بواسطة: Stogbauer, F., وآخرون
  منشور في: (1999)
• A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract
  بواسطة: Willoughby, C, وآخرون
  منشور في: (2003)