Skip to search formSkip to main content

SHFM2 gene

Known as: SHFM2, SHSF2, split hand/foot malformation (ectrodactyly) type 2 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
Split-hand–split-foot malformation (SHFM) is a rare condition that occurs in 1 in 8500–25,000 newborns and accounts for 15% of… Expand
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
2018
2018
Cleft Hand or Split Hand Foot Malformation (SHFM) is a sequence of phenotypes, from a minor shortening of the central digit to a… Expand
Is this relevant?
Review
2015
Review
2015
The split hand/split foot malformation (SHFM), which is also known as ectrodactyly, is a limb malformation syndrome involving the… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
2006
2006
OBJECTIVE To identify the disease-causing genetic alteration of split-hand/split-foot malformation (SHFM) in a Chinese family… Expand
Is this relevant?
2004
2004
Split hand/split foot malformation (SHFM; ectrodactyly) is genetically heterogeneous, with mutations identified at five loci… Expand
Is this relevant?
1995
1995
Ectrodactyly (split hand/split foot malformation, SHSF) is a human limb malformation characterized by absent central digital rays… Expand
Is this relevant?