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Noninvasive screening for prenatal genetic diagnosis.
During the last two decades a number of methods of prenatal diagnosis have become available and have been used either in laboratory research or in routine genetic counselling. Despite the effectiveness of invasive sampling procedures in diagnosing genetic disorders, their use involves some risk. The...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
World Health Organization
1995
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2486681/ https://ncbi.nlm.nih.gov/pubmed/8907774 |
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