Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.
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Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.
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External Links
(P356) |
10.1073/PNAS.85.23.9138
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(P698) |
2973607
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(P819) |
1988PNAS...85.9138P
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(P932) |
282679
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(P5875) |
20181869
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