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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 by Hanifeh Mirtavoos‐Mahyari, Sanaz Ajami, Amirhosein Mehrtash, Seyedeh Mahya Marashiyan, Farbod Bahreini, Kambiz Sheikhy, Sogol Ghanbari, Amin Ardeshirdavani
Published 2022-11-01
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