Genetic regulatory pathways of split-hand/foot malformation
© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd Split-hand/foot malformation (SHFM) is caused by mutations in TP63, DLX5, DLX6, FGF8, FGFR1, WNT10B, and BHLHA9. The clinical features of SHFM caused by mutations of these genes are not distinguishable. This implies that in...
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| Main Authors: | , |
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| Format: | Journal |
| Published: |
2018
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| Subjects: | |
| Online Access: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85053032835&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62597 |
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| Institution: | Chiang Mai University |