Split hand/foot malformation with long bone deficiency associated with BHLHA9 gene duplication: a case report and review of literature
Abstract Background Split hand/foot malformation (SHFM) is a group of congenital skeletal disorders which may occur either as an isolated abnormality or in syndromic forms with extra-limb manifestations. Chromosomal micro-duplication or micro-triplication involving 17p13.3 region has been described...
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Format: | Book |
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BMC,
2019-06-01T00:00:00Z.
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Call Number: |
A1234.567 |
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Copy 1 | Available |