Studies on Effects of Growth Hormone and Insulin-like Growth Factor-I on Dysmorphogenesis in Human Holt-Oram Syndrome by Tbx5 Knockdown Embryonic Zebrafish Model
博士 === 國立陽明大學 === 臨床醫學研究所 === 107 === The Tbx5 mutation in human causes Holt-Oram syndrome, an autosomal dominant disease characterized by a familial history of congenital heart defects and pre-axial radial upper limb defects. Several phenotypes including heart or limb/pectoral fin anomalies consist...
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| Format: | Others |
| Language: | en_US |
| Published: |
2018
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| Online Access: | http://ndltd.ncl.edu.tw/handle/ycegmf |