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Dual fluorescent in situ hybridisation for simultaneous detection of X and Y chromosome-specific probes for the sexing of human preimplantation embryonic nuclei

1 Apr 1992

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Share to Chromosomal and Genetic Variations
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 1577462
DOI: 10.1007/bf00207035

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Dual fluorescent in situ hybridisation for simultaneous detection of X and Y chromosome-specific probes for the sexing of human preimplantation embryonic nucleiPMID 1577462Read ↗

Diagnosis of sex in preimplantation embryos by fluorescent in situ hybridisation.Semantic proximity Read ↗

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Detection of aneuploidy and chromosomal mosaicism in human embryos during preimplantation sex determination by fluorescent in situ hybridisation, (FISH)Semantic proximity Read ↗

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Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogeneticsSemantic proximity Read ↗

Fertilization and early embryology: Diagnosis of major chromosome aneuploidies in human preimplantation embryosSemantic proximity Read ↗

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