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HGG Advances
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December 10, 2021
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease
Polakit Teekakirikul, Wenjuan Zhu, George C Gabriel, et al.
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Search research articles
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Showing results (31-40 of 31) with videos related to
Sort By:
Page
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This site can display upto 31 results.
HGG Advances
|
December 10, 2021
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease
Polakit Teekakirikul, Wenjuan Zhu, George C Gabriel, et al.
Page
of 4