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Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project.

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Title: Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project.
Authors: Ferlini, Alessandra1 (AUTHOR) fla@unife.it, Gross, Edith Sky2 (AUTHOR), Garnier, Nicolas3 (AUTHOR), Berghout, Joanne (AUTHOR), Zygmunt, Aldona (AUTHOR), Singh, Deependra (AUTHOR), Huang, Kui A. (AUTHOR), Kantz, Waltraud (AUTHOR), Blankart, Carl Rudolf (AUTHOR), Gillner, Sandra (AUTHOR), Zhao, Jiawei (AUTHOR), Roettger, Richard (AUTHOR), Saier, Christina (AUTHOR), Kirschner, Jan (AUTHOR), Schenk, Joern (AUTHOR), Atkins, Leon (AUTHOR), Ryan, Nuala (AUTHOR), Zarakowska, Kaja (AUTHOR), Zschüntzsch, Jana (AUTHOR), Zuccolo, Michela (AUTHOR)
Source: Orphanet Journal of Rare Diseases. 10/4/2023, Vol. 18 Issue 1, p1-4. 4p.
Database: Academic Search Ultimate
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An: 172777770
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  Data: Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project.
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  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 10/4/2023, Vol. 18 Issue 1, p1-4. 4p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=172777770
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              Text: 10/4/2023
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