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

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References

  1. Lunke, S. et al. Nat. Med. https://doi.org/10.1038/s41591-023-02401-9 (2023).

    Article  PubMed  PubMed Central  Google Scholar 

  2. Dimmock, D. et al. Am. J. Hum. Genet. 108, 1231–1238 (2021).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Wu, B. et al. Crit. Care Med. 49, 1674–1683 (2021).

    Article  CAS  PubMed  Google Scholar 

  4. Krantz, I. et al. JAMA Pediatr. 175, 1218–1226 (2021).

    Article  PubMed  Google Scholar 

  5. Kingsmore, S. & Cole, F. Annu. Rev. Genomics Hum. Genet. 23, 427–448 (2022).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Kingsmore, S. Cold Spring Harb. Mol. Case Stud. 8, a006204 (2022).

    Article  PubMed  PubMed Central  Google Scholar 

  7. Anonymous. Medica Magazine https://go.nature.com/3thx8dT (26 April 2022).

  8. Scott, E. et al. Nat. Genet. 48, 1071–1076 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. El Naofal, M. et al. Genome Med. 15, 5 (2023).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Halabi, N. et al. Genome Med. 14, 56 (2022).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

The Little Falcon study is co-sponsored by Al Jalila Children’s Specialty Hospital, Dubai, UAE, and Illumina, San Diego, CA, USA.

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Correspondence to Ahmad N. Abou Tayoun.

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The authors’ Little Falcon study receives sponsorship funding from Illumina.

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Abou Tayoun, A.N., Alsheikh-Ali, A. A rapid whole-genome sequencing service for infants with rare diseases in the United Arab Emirates. Nat Med 29, 2979–2980 (2023). https://doi.org/10.1038/s41591-023-02596-x

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  • DOI: https://doi.org/10.1038/s41591-023-02596-x

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