Exclusion of linkage between autosomal dominant split hand/split foot and markers from chromosome 7q: further evidence for genetic heterogeneity.

Míreanna Comhchosúla

• Fine mapping of the Autosomal Dominant Split Hand/Split Foot Locus on Chromosome 7, Band q21.3-q22.1
  le: Scherer, Stephen W., et al.
  Foilsithe: (1994)
• Heterogeneity of the autosomal dominant split hand/split foot malformation.
  le: Zlotogora, J
  Foilsithe: (1995)
• Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformation.
  le: Palmer, S. E., et al.
  Foilsithe: (1994)
• Is there an autosomal recessive form of the split hand and split foot malformation?
  le: Zlotogora, J, et al.
  Foilsithe: (1989)
• Isolated autosomal dominant type E brachydactyly: exclusion of linkage to candidate regions 2q37 and 20q13.
  le: Oude Luttikhuis, M E, et al.
  Foilsithe: (1996)