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47. Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. Pinkel D, Landegent J, Collins C, Fuscoe J, Segraves R, Lucas J, Gray J. Proc Natl Acad Sci U S A; 1988 Dec 23; 85(23):9138-42. PubMed ID: 2973607 [Abstract] [Full Text] [Related]
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