Chromosome in situ suppression hybridisation in human male meiosis.

Author:

Goldman A S,Hulten M A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference27 articles.

1. Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization;Pinkel, D.; Straume, T.; Gray, J.W.;Proc Natl Acad Sci USA,1986

2. Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries;Lichter, P.; Cremer, T.; Borden, J.; Manuelidis, L.; Ward, D.C.;Hum Genet,1988

3. Construction of gene libraries for each human chromosome;MA, Van Dilla; LL, Deaven;Cytometry,1990

4. Construction of fifteen human chromosome-specific DNA libraries from flow-purified chromosomes;Fuscoe, J.C.; Clark, L.M.; Van Dilla, M.A.;Cytogenet Cell Genet,1986

5. Cytogenetic analysis by in situ hybridization with fluorescently labelled nucleic acid probes;Pinkel, D.; Gray, J.W.; Trask, B.; van den Engh, G.; Fuscoe, J.; van Dekken, H.;Cold Spring Harbor Symp Quant Biol,1986

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