SPLIT-HAND/FOOT MALFORMATION 5 (disorder)

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

Topic mentions per year

Topic mentions per year

2004-2012
012320042012

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… (More)
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2012
2012
Split-hand/foot malformation (SHFM) is a rare limb developmental malformation, characterized by variable degree of median clefts… (More)
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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… (More)
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2010
2010
Background: Deletions that encompass 2q31.1 have been proposed as a microdeletion syndrome with common clinical features… (More)
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Review
2008
Review
2008
BACKGROUND Split hand foot malformation (SHFM) (cleft hand, central ray deficiency) is a highly variable malformation that shows… (More)
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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… (More)
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2006
2006
Split-hand/split-foot malformation (SHFM, also called ectrodactyly) is a clinically variable and genetically heterogeneous group… (More)
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2006
2006
Split-hand/foot malformation (SHFM), or ectrodactyly, is characterized by underdeveloped or absent central digital rays, clefts… (More)
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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… (More)
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2004
2004
Split hand/split foot malformation (SHFM; ectrodactyly) is genetically heterogeneous, with mutations identified at five loci… (More)
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