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Whole-exome sequencing reveals a combination of extremely rare single-nucleotide polymorphism of DNAH9 and RSPH1 genes in a Japanese fetus with situs viscerum inversus

Crossref DOI link: https://doi.org/10.1007/s00795-021-00287-5

Published Online: 2021-05-18

Published Print: 2021-09

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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