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ArticleHuman genome variation2021

Estimation of the carrier frequencies and proportions of potential patients by detecting causative gene variants associated with autosomal recessive bone dysplasia using a whole-genome reference panel of Japanese individuals.

Shinichi Nagaoka et al.PubMed ↗Full text ↗Publisher ↗

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2023
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Full record →Abstract, authors, funding and every citing paper · PMID 33452237