Split hand/foot malformation syndrome (SHFM): rare congenital orthopaedic disorder

Similar Items

• Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25.
  od: Raas-Rothschild, A, i dr.
  Izdano: (1996)
• Genetic analysis of a congenital split-hand/split-foot malformation 4 pedigree
  od: Yang, Xiao, i dr.
  Izdano: (2018)
• Is there an autosomal recessive form of the split hand and split foot malformation?
  od: Zlotogora, J, i dr.
  Izdano: (1989)
• Heterogeneity of the autosomal dominant split hand/split foot malformation.
  od: Zlotogora, J
  Izdano: (1995)
• Split hand/foot malformation due to chromosome 7q aberrations(SHFM1): additional support for functional haploinsufficiency as the causative mechanism
  od: van Silfhout, Anneke T, i dr.
  Izdano: (2009)