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Maternal Consequences of the Detection of Fragile X Carriers in Newborn Screening
OBJECTIVES: The possibility of newborn screening for fragile X syndrome is complicated by the potential for identifying premutation carriers. Although knowing the child’s carrier status has potential benefits, the possibility of late-onset disorders in carrier children and their parents raises conce...
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| Veröffentlicht in: | Pediatrics |
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| Hauptverfasser: | , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
American Academy of Pediatrics
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4516945/ https://ncbi.nlm.nih.gov/pubmed/26169437 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1542/peds.2015-0414 |
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