Newborn screening for rare diseases: expanding the paradigm in the genomic era.
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| Title: | Newborn screening for rare diseases: expanding the paradigm in the genomic era. |
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| Authors: | Grošelj U; University Medical Centre Ljubljana, University Children's Hospital, Ljubljana, Slovenia.; Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia. |
| Source: | Journal of perinatal medicine [J Perinat Med] 2025 Sep 29; Vol. 54 (1), pp. 116-122. Date of Electronic Publication: 2025 Sep 29 (Print Publication: 2026). |
| Publication Type: | Journal Article; Review |
| Journal Info: | Publisher: Walter De Gruyter Country of Publication: Germany NLM ID: 0361031 Publication Model: Electronic-Print Cited Medium: Internet ISSN: 1619-3997 (Electronic) Linking ISSN: 03005577 NLM ISO Abbreviation: J Perinat Med Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1619-3997 |
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| DOI: | 10.1515/jpm-2025-0363 |
