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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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2012
2012
Split-hand/foot malformation (SHFM) is a rare limb developmental malformation, characterized by variable degree of median clefts… Expand
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2011
2011
Split hand/foot malformation (SHFM) is characterized by underdeveloped or absent central digital rays, clefts of hands and feet… Expand
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2011
2011
INTRODUCTION The clinical phenotype of the chromosome 2q31 deletion syndrome consists of limb anomalies ranging from… Expand
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2010
2010
Background: Deletions that encompass 2q31.1 have been proposed as a microdeletion syndrome with common clinical features… Expand
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2006
2006
Split-hand/split-foot malformation (SHFM, also called ectrodactyly) is a clinically variable and genetically heterogeneous group… Expand
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2006
2006
Split-hand/foot malformation (SHFM), or ectrodactyly, is characterized by underdeveloped or absent central digital rays, clefts… Expand
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2006
2006
OBJECTIVE To identify the disease-causing genetic alteration of split-hand/split-foot malformation (SHFM) in a Chinese family… Expand
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2005
2005
OBJECTIVES To describe and discuss the clinical, cytogenetic and molecular findings in a fetus with the first prenatally detected… Expand
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2004
2004
Split hand/split foot malformation (SHFM; ectrodactyly) is genetically heterogeneous, with mutations identified at five loci… Expand
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2003
2003
Ectrodactyly or split hand/foot malformation (SHFM) is a human limb malformation characterised by underdevelopment or absence of… Expand
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