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- W2138086044 abstract "In situ hybridization was used to characterize an undetected chromosome translocation in a child whose metaphase chromosome analysis in peripheral blood and in skin culture revealed apparent monosomy 21. The cytogenetic study revealed 45 chromosomes, and no other structural anomalies were detected with G banding. In situ hybridization of chromosome 21-specific probes to metaphase chromosomes and reverse banding from the proband showed a de novo translocation between chromosome 5 and chromosome 21." @default.
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- W2138086044 date "1993-02-01" @default.
- W2138086044 modified "2023-10-13" @default.
- W2138086044 title "De novo t(5p;21q) in a patient previously diagnosed as monosomy 21" @default.
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- W2138086044 doi "https://doi.org/10.1111/j.1399-0004.1993.tb04457.x" @default.
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