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SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations
Preimplantation genetic diagnosis (PGD) for chromosomal rearrangements (CR) is mainly based on fluorescence in situ hybridisation (FISH). Application of this technique is limited by the number of available fluorochromes, the extensive preclinical work-up and technical and interpretative artefacts. W...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3421116/ https://ncbi.nlm.nih.gov/pubmed/22378284 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2012.27 |
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