Chromosome in situ suppression hybridisation in clinical cytogenetics.
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M. Hultén | J. Waters | C. Gould | A. S. Goldman | M. Hultén | C P Gould | A S Goldman | J J Waters
[1] A. Hamosh,et al. The Marfan syndrome locus: confirmation of assignment to chromosome 15 and identification of tightly linked markers at 15q15-q21.3. , 1991, Genomics.
[2] J. Wiegant,et al. Detection of the Philadelphia chromosome in interphase nuclei. , 1990, Cytogenetics and cell genetics.
[3] D. Pinkel,et al. Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[4] D. Ward,et al. Rapid detection of human chromosome 21 aberrations by in situ hybridization. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[5] D. Pinkel,et al. Fluorescence insitu hybridization withhumanchromosome-specific libraries: Detection oftrisomy 21andtranslocations of chromosome 4 , 1988 .
[6] A. Emery,et al. Human Cytogenetics. A Practical Approach , 1987 .