12 Chromosome Analysis by Fluorescence in situ Hybridization
185
Lichter P, Cremer T, Borden J, Manuelidis L, Ward DC (1988) Delineation of individual
human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries. Hum Genet 80: 224-234
Lichter P, Ward DC (1990) Is non-isotopic in situ hybridization fmally coming of age?
Nature 345: 93-95
Manuelidis L ( 1985) In situ detection ofDNA sequences using biotinylated probes. Focus
7:4-8
Nederlof PM, Flier van der S, Vrolijk J, Tanke HJ, RaapAK (1992) Fluorescence ratio
measurements of double-labeled probes for multiple in situ hybridization by digital
imaging microscopy. Cytometry 13: 839-845
Pinkel D, Gray JW, Trask B, van den Engh G, Fuscoe J, van Dekken H (1986) Cytogenetic
analysis by in situ hybridization with fluorescently labeled nucleic acid probes. Cold
Spring Rarbor Symp Quant Biol 51: 151-157
Pinkel D, Landegent J, Collins C, Fuscoe J, Segraves R, Lucas J, Gray JW (1988) Fluorescence in situ hybridization with human chromosome-specific libraries: detection of
trisomy 21 and translocations of chromosome 4. Proc Natl Acad Sei USA 85: 91389142
Raap AK, Dirks RW, Jiwa NM, NederlofPM, van der Ploeg M (1990) In situ hybridization
withhapten-modified DNA probes. In: RaczP, Haase AT, Gluckman JC (eds) Modern
Pathology of AIDS and Other Retroviral Infections. S. Karger, Basel
Ried T, Landes G, Dackowski W, Klinger K, Ward D (1992) Multicolor fluorescence in
situ hybridization for the simultaneous detection of probe sets for chromosome 13, 18,
21, X and Y in uneuhured amniotic fluid cells. Hum Molec Genet 1: 307-313
Rooney DE, Czepulkowski (1992) Human Cytogenetics - A practical approach, Vol I
Oxford University, Oxford 157-192
Schröck E, Du Manoir S, Veldman T, Schoell B, Wienberg H, Ferguson-Smith, MA, Ning
Y, Ledbetter DH; Bar-Am I Soenksen D, Garini Y, Ried T (1996) Multicolor spectral
caryotyping of human chromosomes. Science 273: 494-498
Speicher MR, Ballard SG, Ward DC (1996) Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nature Genet 12: 368-375
Trask B (1991) Fluorescence in situ hybridization: applications in cytogenetics and gene
mapping. TIG 7: 149-154
Stilgenbauer S, Döhner H, Bulgay-Mörschel M, Weitz S, Bentz M, Licher P (1993) High
frequency of monoalleHe retinoblastoma gene deletion in B-Cell chronic lymphoid
leukemia shown by interphase cytogenetics. Blood 81: 2118-2124
Wiegant J, Ried T, NederlofP, van der Ploeg M, Tanke HJ, RaapAK (1991) In situ hybridization with fluoresceinated DNA. Nucleic Acids Res 19: 3237-3241
Zirbel RM, Mathieu UR, Kurz A, Cremer T, Lichter P (1993) Evidence for a nuclear compartment of transcription and splicing located at chromosome domain boundaries.
Chromosome Research 1:93-106
185
Lichter P, Cremer T, Borden J, Manuelidis L, Ward DC (1988) Delineation of individual
human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries. Hum Genet 80: 224-234
Lichter P, Ward DC (1990) Is non-isotopic in situ hybridization fmally coming of age?
Nature 345: 93-95
Manuelidis L ( 1985) In situ detection ofDNA sequences using biotinylated probes. Focus
7:4-8
Nederlof PM, Flier van der S, Vrolijk J, Tanke HJ, RaapAK (1992) Fluorescence ratio
measurements of double-labeled probes for multiple in situ hybridization by digital
imaging microscopy. Cytometry 13: 839-845
Pinkel D, Gray JW, Trask B, van den Engh G, Fuscoe J, van Dekken H (1986) Cytogenetic
analysis by in situ hybridization with fluorescently labeled nucleic acid probes. Cold
Spring Rarbor Symp Quant Biol 51: 151-157
Pinkel D, Landegent J, Collins C, Fuscoe J, Segraves R, Lucas J, Gray JW (1988) Fluorescence in situ hybridization with human chromosome-specific libraries: detection of
trisomy 21 and translocations of chromosome 4. Proc Natl Acad Sei USA 85: 91389142
Raap AK, Dirks RW, Jiwa NM, NederlofPM, van der Ploeg M (1990) In situ hybridization
withhapten-modified DNA probes. In: RaczP, Haase AT, Gluckman JC (eds) Modern
Pathology of AIDS and Other Retroviral Infections. S. Karger, Basel
Ried T, Landes G, Dackowski W, Klinger K, Ward D (1992) Multicolor fluorescence in
situ hybridization for the simultaneous detection of probe sets for chromosome 13, 18,
21, X and Y in uneuhured amniotic fluid cells. Hum Molec Genet 1: 307-313
Rooney DE, Czepulkowski (1992) Human Cytogenetics - A practical approach, Vol I
Oxford University, Oxford 157-192
Schröck E, Du Manoir S, Veldman T, Schoell B, Wienberg H, Ferguson-Smith, MA, Ning
Y, Ledbetter DH; Bar-Am I Soenksen D, Garini Y, Ried T (1996) Multicolor spectral
caryotyping of human chromosomes. Science 273: 494-498
Speicher MR, Ballard SG, Ward DC (1996) Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nature Genet 12: 368-375
Trask B (1991) Fluorescence in situ hybridization: applications in cytogenetics and gene
mapping. TIG 7: 149-154
Stilgenbauer S, Döhner H, Bulgay-Mörschel M, Weitz S, Bentz M, Licher P (1993) High
frequency of monoalleHe retinoblastoma gene deletion in B-Cell chronic lymphoid
leukemia shown by interphase cytogenetics. Blood 81: 2118-2124
Wiegant J, Ried T, NederlofP, van der Ploeg M, Tanke HJ, RaapAK (1991) In situ hybridization with fluoresceinated DNA. Nucleic Acids Res 19: 3237-3241
Zirbel RM, Mathieu UR, Kurz A, Cremer T, Lichter P (1993) Evidence for a nuclear compartment of transcription and splicing located at chromosome domain boundaries.
Chromosome Research 1:93-106