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Prenatal Diagnosis by Chromosomal Microarray Analysis
Chromosomal microarray analysis (CMA) is performed either by array comparative genomic hybridization (aCGH) or by using a SNP array. In the prenatal setting, CMA is on par with traditional karyotyping for detection of major chromosomal imbalances such as aneuploidy and unbalanced rearrangements. CMA...
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| Publicado no: | Fertil Steril |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5856154/ https://ncbi.nlm.nih.gov/pubmed/29447663 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.fertnstert.2018.01.005 |
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