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Simultaneous Detection of Chromosomes X, Y, 13, 18, and 21 by Fluorescence In Situ Hybridization in Blastomeres Obtained from Preimplantation Embryos
Purpose.Simultaneous fluorescence in situ hybridization (FISH) was used in a preimplantation genetic diagnosis program to determine which embryos were normal for chromosomes X, Y, 13, 18, and 21. Methods:Single blastomeres were disrupted and attached to glass slides using acetic acid and ethanol. Us...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Kluwer Academic Publishers-Plenum Publishers
1998
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3454756/ https://ncbi.nlm.nih.gov/pubmed/9604767 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1023/A:1022504829854 |
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