D. Tkachuk

Libraries for each human chromosome, constructed from sorter-enriched chromosomes by using linker-adaptor PCR.

D. Pinkel, J. Gray, M. Vooijs, 1993, American journal of human genetics.

Clinical applications of fluorescence in situ hybridization.

H U Weier, J W Gray, D Pinkel, 1991, Genetic analysis, techniques and applications.

Analytical approaches to detection and characterization of disease-linked chromosome aberrations.

B. Trask, G. van den Engh, W. Kuo, 1990, Bone marrow transplantation.

Detection of bcr-abl fusion in chronic myelogeneous leukemia by in situ hybridization

D Pinkel, D. Pinkel, J. Gray, 1990, Science.

Simple repeated sequences in human satellite DNA.

M. Frommer, A. Reisner, P. Vincent, 1982, Nucleic acids research.

2 Molecular cytogenetic analysis of chromosome aberrations

W. Kuo, D. Pinkel, J. Gray, 1992 .

HRX involvement in de novo and secondary leukemias with diverse chromosome 11q23 abnormalities.

M. Amylon, M. Cleary, S. Hunger, 1993, Blood.

Applications of fluorescence in situ hybridization in biological dosimetry and detection of disease-specific chromosome aberrations.

W. Kuo, D. Pinkel, O. Kallioniemi, 1991, Progress in clinical and biological research.