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Women’s experiences receiving abnormal prenatal chromosomal microarray testing results
PURPOSE: Genomic microarrays can detect copy number variants not detectable by conventional cytogenetics. This technology is diffusing rapidly into prenatal settings even though the clinical implications of many copy number variants are currently unknown. We conducted a qualitative pilot study to ex...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2012
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3877835/ https://ncbi.nlm.nih.gov/pubmed/22955112 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2012.113 |
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