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Comment
. 2023 Jun 1;110(6):1017.
doi: 10.1016/j.ajhg.2023.05.004.

Response to Grosse et al

Affiliations
Comment

Response to Grosse et al

Stephen F Kingsmore et al. Am J Hum Genet. .
No abstract available

PubMed Disclaimer

Comment on

  • Progress in expanding newborn screening in the United States.
    Grosse SD, Cuthbert C, Gaffney M, Gaviglio A, Hinton CF, Kellar-Guenther Y, Kemper AR, McKasson S, Ojodu J, Riley C, Singh S, Sontag MK, Shapira SK. Grosse SD, et al. Am J Hum Genet. 2023 Jun 1;110(6):1015-1016. doi: 10.1016/j.ajhg.2023.05.002. Am J Hum Genet. 2023. PMID: 37267896 Free PMC article. No abstract available.

References

    1. Kingsmore S.F., Smith L.D., Kunard C.M., Bainbridge M., Batalov S., Benson W., Blincow E., Caylor S., Chambers C., Del Angel G., et al. A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases. Am. J. Hum. Genet. 2022;109:1605–1619. - PMC - PubMed
    1. Kingsmore S.F., BeginNGS Consortium Rapid newborn genome sequencing to end the diagnostic and therapeutic odyssey. Am. J. Med. Genet. C Semin. Med. Genet. 2022;190:243–256. - PMC - PubMed
    1. Singh S., Ojodu J., Kemper A.R., Lam W.K.K., Grosse S.D. Implementation of Newborn Screening for Conditions in the United States First Recommended during 2010-2018. Int. J. Neonatal Screen. 2023;9:20. - PMC - PubMed
    1. Bick D., Bick S.L., Dimmock D.P., Fowler T.A., Caulfield M.J., Scott R.H. An online compendium of treatable genetic disorders. Am. J. Med. Genet. C Semin. Med. Genet. 2021;187:48–54. - PMC - PubMed
    1. Yu T.W., Kingsmore S.F., Green R.C., MacKenzie T., Wasserstein M., Caggana M., Gold N.B., Kennedy A., Kishnani P.S., Might M., et al. Are we prepared to deliver gene-targeted therapies for rare diseases? Am. J. Med. Genet. C Semin. Med. Genet. 2023;193:7–12. - PubMed

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