Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

SPLIT-HAND/FOOT MALFORMATION 5 (disorder)

Known as: Split-Hand-Foot Malformation 5, SPLIT-HAND/FOOT MALFORMATION 5, SHFM5 
Split-hand/foot malformation mapped to chromosome 2q31.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2012
2012
Khan S, Basit S, Zimri FK, Ali N, Ali G, Ansar M, Ahmad W. A novel homozygous missense mutation in WNT10B in familial split‐hand… Expand
2011
2011
Split hand/foot malformation (SHFM) is characterized by underdeveloped or absent central digital rays, clefts of hands and feet… Expand
2010
2010
Introduction The clinical phenotype of the chromosome 2q31 deletion syndrome consists of limb anomalies ranging from… Expand
2010
2010
Background: Deletions that encompass 2q31.1 have been proposed as a microdeletion syndrome with common clinical features… Expand
  • figure 1
  • table 1
  • figure 2
  • figure 3
2006
2006
Split‐hand/split‐foot malformation (SHFM, also called ectrodactyly) is a clinically variable and genetically heterogeneous group… Expand
2006
2006
Split‐hand/foot malformation (SHFM), or ectrodactyly, is characterized by underdeveloped or absent central digital rays, clefts… Expand
2006
2006
OBJECTIVE To identify the disease-causing genetic alteration of split-hand/split-foot malformation (SHFM) in a Chinese family… Expand
2005
2005
To describe and discuss the clinical, cytogenetic and molecular findings in a fetus with the first prenatally detected… Expand
2004
2004
Split hand/split foot malformation (SHFM; ectrodactyly) is genetically heterogeneous, with mutations identified at five loci… Expand
2003
2003
Ectrodactyly or split hand/foot malformation (SHFM) is a human limb malformation characterised by underdevelopment or absence of… Expand