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Assessment of efficacy of prenatal genetic diagnosis for fragile X syndrome using nested PCR
Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability and the leading monogenic cause of autism spectrum disorder. It has previously been demonstrated that prenatal genetic diagnosis is efficient for the diagnosis of FXS. The present study investigated the diagnostic...
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| Publicado no: | Exp Ther Med |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5958809/ https://ncbi.nlm.nih.gov/pubmed/29844802 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2018.6060 |
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