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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

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Review
2013
Review
2013
Split-hand/foot malformation (SHFM) is a congenital limb defect affecting predominantly the central rays of the autopod and… 
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… 
2010
2010
Introduction The clinical phenotype of the chromosome 2q31 deletion syndrome consists of limb anomalies ranging from… 
2010
2010
Background: Deletions that encompass 2q31.1 have been proposed as a microdeletion syndrome with common clinical features… 
Review
2008
Review
2008
BACKGROUND Split hand foot malformation (SHFM) (cleft hand, central ray deficiency) is a highly variable malformation that shows… 
2006
2006
Split‐hand/split‐foot malformation (SHFM, also called ectrodactyly) is a clinically variable and genetically heterogeneous group… 
2006
2006
Split‐hand/foot malformation (SHFM), or ectrodactyly, is characterized by underdeveloped or absent central digital rays, clefts… 
2005
2005
To describe and discuss the clinical, cytogenetic and molecular findings in a fetus with the first prenatally detected… 
2004
2004
Split hand/split foot malformation (SHFM; ectrodactyly) is genetically heterogeneous, with mutations identified at five loci… 
2003
2003
Ectrodactyly or split hand/foot malformation (SHFM) is a human limb malformation characterised by underdevelopment or absence of…