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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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Autors principals: Smith, Scott E., Toledo, Andrew A., Massey, Joe B., Kort, Hilton I.
Format: Artigo
Idioma:Inglês
Publicat: Kluwer Academic Publishers-Plenum Publishers 1998
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Accés en línia: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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