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Are We Ready for Fragile X Newborn Screening Testing?—Lessons Learnt from a Feasibility Study
Fragile X syndrome (FXS) is the most prevalent heritable cause of cognitive impairment but is not yet included in a newborn screening (NBS) program within Australia. This paper aims to assess the feasibility and reliability of population screening for FXS using a pilot study in one hospital. A total...
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| Gepubliceerd in: | Int J Neonatal Screen |
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| Hoofdauteurs: | , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
MDPI
2018
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7548904/ https://ncbi.nlm.nih.gov/pubmed/33072935 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijns4010009 |
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