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Comment
. 2023 Dec;29(12):2979-2980.
doi: 10.1038/s41591-023-02596-x.

A rapid whole-genome sequencing service for infants with rare diseases in the United Arab Emirates

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Comment

A rapid whole-genome sequencing service for infants with rare diseases in the United Arab Emirates

Ahmad N Abou Tayoun et al. Nat Med. 2023 Dec.
No abstract available

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Comment on

  • Integrated multi-omics for rapid rare disease diagnosis on a national scale.
    Lunke S, Bouffler SE, Patel CV, Sandaradura SA, Wilson M, Pinner J, Hunter MF, Barnett CP, Wallis M, Kamien B, Tan TY, Freckmann ML, Chong B, Phelan D, Francis D, Kassahn KS, Ha T, Gao S, Arts P, Jackson MR, Scott HS, Eggers S, Rowley S, Boggs K, Rakonjac A, Brett GR, de Silva MG, Springer A, Ward M, Stallard K, Simons C, Conway T, Halman A, Van Bergen NJ, Sikora T, Semcesen LN, Stroud DA, Compton AG, Thorburn DR, Bell KM, Sadedin S, North KN, Christodoulou J, Stark Z. Lunke S, et al. Nat Med. 2023 Jul;29(7):1681-1691. doi: 10.1038/s41591-023-02401-9. Epub 2023 Jun 8. Nat Med. 2023. PMID: 37291213 Free PMC article.

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