Maian Roifman
2PUBLICATIONS
2CO-AUTHORS
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Publications (2)
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|Feb 25, 2021
Heterozygous NOTCH1 deletion associated with variable congenital heart defects.Maian Roifman, Brian Hon Yin Chung, Diane Myles Reid
|Sep 05, 2020
Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiency.Maian Roifman, Kirsten M Niles, Lauren MacNeil
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