Sogol Ghanbari
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1CO-AUTHORS

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Publications (1)
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|Nov 18, 2022
Clinical whole-exome sequencing analysis reveals a novel missense COL11A1 mutation resulting in an 18-week Iranian male aborted fetus with Fibrochondrogenesis 1: A case report.Hanifeh Mirtavoos-Mahyari, Sanaz Ajami, Amirhosein Mehrtash
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