Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation
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DOI: 10.1590/1678-4685-gmb-2016-0162
Abstract: Abstract Split-hand/split-foot malformation (SHFM), also known as ectrodactyly is a rare genetic disorder. It is a clinically and genetically heterogeneous group of limb malformations characterized by absence/hypoplasia and/or median cleft of hands and/or feet. To… read more here.
Keywords: foot malformation; gene; wnt10b gene; split hand ... See more keywords