TREAT: systematic and inclusive selection process of genes for genomic newborn screening as part of the Screen4Care project.
- DOI
- 10.1186/s13023-025-03692-6
- Published
- 2025 May 15
- Container
- Orphanet journal of rare diseases
- Publisher
- Not recorded
- Open access
- yes
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limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-025-03692-6,
title = {TREAT: systematic and inclusive selection process of genes for genomic newborn screening as part of the Screen4Care project.},
author = {Saier C and Sansen S and Berghout J and Freyler K and Einhorn M and Einhorn Y and Matalonga L and Beltran S and Novelli A and Selvatici R and Fortunato F and Montanari S and Martinez-Fresno M and Gumus G and Agolini E and Garnier N and Ferlini A and Bertini E and Kirschner J},
year = {2025},
journal = {Orphanet journal of rare diseases},
doi = {10.1186/s13023-025-03692-6},
url = {https://doi.org/10.1186/s13023-025-03692-6}
}RIS
TY - JOUR TI - TREAT: systematic and inclusive selection process of genes for genomic newborn screening as part of the Screen4Care project. AU - Saier C AU - Sansen S AU - Berghout J AU - Freyler K AU - Einhorn M AU - Einhorn Y AU - Matalonga L AU - Beltran S AU - Novelli A AU - Selvatici R AU - Fortunato F AU - Montanari S AU - Martinez-Fresno M AU - Gumus G AU - Agolini E AU - Garnier N AU - Ferlini A AU - Bertini E AU - Kirschner J PY - 2025 JO - Orphanet journal of rare diseases DO - 10.1186/s13023-025-03692-6 UR - https://doi.org/10.1186/s13023-025-03692-6 ER -
APA
C, S., S, S., J, B., K, F., M, E., Y, E., L, M., S, B., A, N., R, S., F, F., S, M., M, M., G, G., E, A., N, G., A, F., E, B., & J, K. (2025). TREAT: systematic and inclusive selection process of genes for genomic newborn screening as part of the Screen4Care project.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-025-03692-6
Source records
- pubmed · retrieved 2026-09-26T13:17:23.765Z