1 FISH Techniques, FISH Probes and Their Applications in Medicine and Biology - An Overview
47
Nishizaki T, Chew K, Chu L, Isola J, Kallioniemi A, Weidner N, Waldman FM (1997)
Genetic alterations in lobular breast cancer by comparative genomic hybridization.
Int J Cancer 74:513-517
Novelli A, Sabani M, Caiola A, Digilio MC, Giannotti A, Mingarelli R, Novelli G, Dallapiccola B (1999) Diagnosis of DiGeorge and Williams syndromes using FISH analysis of peripheral blood smears. Mol Cell Probes 4:303-307
Nowell PC, Hungerford DA (1960) A minute chromosome in human chronic granulocytic leukemia. Science 132:1497-1499
OMIM - On line Mendelian Inheritance in Man: http://www.ncbi.nih.gov/Omim/
Para I, Windle B (1993) High resolution visual mapping of stretched DNA by fluorescent in situ hybridization. Nat Genet 5:17-21
Patau K, Smith DW, Therman E, Inhorn SL, Wagner HP (1960) Multiple congenital
anomaly caused by an extra autosome. Lancet 1:790-793
Pierce KE, Fitzgerald LM, Seibel MM, Zilberstein M (1998) Preimplantation genetic
diagnosis of chromosome balance in embryos from a patient with a balanced reciprocal translocation. Molec Hum Reprod 4:167-172
Pinkel D, Straume T, Gray JW (1986) Cytogenetic analysis using quantitative, highsensitivity, fluorescence hybridization. Proc Natl Acad Sci USA 83:2934-2938
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 translocation of chromosome 4. Proc Nat! Acad Sci USA 85:91389142
Rao PH, Cigudosa JC, Ning Y, Calasanz MJ, Iida S, Tagawa S, Michaeli J, Klein B, DallaFavera R, Jhanwar SC, Ried T, Chaganti RS (1998) Multicolor spectral karyotyping
identifies new recurring breakpoints and translocations in multiple myeloma. Blood
92:1743-1748
Raap AK, Florijn RJ, Blonden LAJ, Wiegant JCAG, Vaandrager JW. Vrolijk J, den Dunnen J, Tanke HJ, van Ommen GJB (1996) Fiber-FISH as a DNA mapping tool. Methods Enzymol 9:67-73
Ried T, Baldini A, Rand TC, Ward DC (1992) Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and
digital imaging microscopy. Proc Nat! Acad Sci USA 89:1388-1392
Roberts I, Wienberg 1, Nacheva E, Grace C, Griffin D, Coleman N (1999) Novel method
for the production of multiple colour chromosome paints for use in karyotyping by
fluorescence in situ hybridisation. Genes Chromsom Cancer 25:241-250
Roux W (1883) Uber die Bedeutung der Kerntheilungsfiguren, Engelmann, Leipzig.
Rowley JD, Diaz MO, Espinosa R, Patel YD, van Melle E, Ziemin S, Taillon-Miller P et al
(1990) Mapping chromosome band llq23 in human acute leukemia with biotinylated probes: identification of 11q23 translocation breakpoints with a yeast artificial
chromosome. Proc Nat! Acad Sci USA 87:9358-9362
Rubin CM, Carrino JJ, Dickler MN, Leibowitz D, Smith SD, Westbrook CA (1988) Heterogeneity of genomic fusion of BCR and ABL in Philadelphia chromosome-positive
acute lymphoblastic leukemia. Proc Nat! Acad Sci USA 85:2795-2799
Saiki RK, Scharf S, Faloona F, Mullis KB, Horn GT, Erlich HA, Arnheim N (1985) Enzymatic amplification ofbeta-globin genomic sequences and restriction site analysis
for diagnosis of sickle cell anemia. Science 230:1350-1354
Schinzel A (1983) Catalog of unbalanced chromosome aberrations in man. Walter de
Gruyter and Co. Berlin, pp 1.7
47
Nishizaki T, Chew K, Chu L, Isola J, Kallioniemi A, Weidner N, Waldman FM (1997)
Genetic alterations in lobular breast cancer by comparative genomic hybridization.
Int J Cancer 74:513-517
Novelli A, Sabani M, Caiola A, Digilio MC, Giannotti A, Mingarelli R, Novelli G, Dallapiccola B (1999) Diagnosis of DiGeorge and Williams syndromes using FISH analysis of peripheral blood smears. Mol Cell Probes 4:303-307
Nowell PC, Hungerford DA (1960) A minute chromosome in human chronic granulocytic leukemia. Science 132:1497-1499
OMIM - On line Mendelian Inheritance in Man: http://www.ncbi.nih.gov/Omim/
Para I, Windle B (1993) High resolution visual mapping of stretched DNA by fluorescent in situ hybridization. Nat Genet 5:17-21
Patau K, Smith DW, Therman E, Inhorn SL, Wagner HP (1960) Multiple congenital
anomaly caused by an extra autosome. Lancet 1:790-793
Pierce KE, Fitzgerald LM, Seibel MM, Zilberstein M (1998) Preimplantation genetic
diagnosis of chromosome balance in embryos from a patient with a balanced reciprocal translocation. Molec Hum Reprod 4:167-172
Pinkel D, Straume T, Gray JW (1986) Cytogenetic analysis using quantitative, highsensitivity, fluorescence hybridization. Proc Natl Acad Sci USA 83:2934-2938
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 translocation of chromosome 4. Proc Nat! Acad Sci USA 85:91389142
Rao PH, Cigudosa JC, Ning Y, Calasanz MJ, Iida S, Tagawa S, Michaeli J, Klein B, DallaFavera R, Jhanwar SC, Ried T, Chaganti RS (1998) Multicolor spectral karyotyping
identifies new recurring breakpoints and translocations in multiple myeloma. Blood
92:1743-1748
Raap AK, Florijn RJ, Blonden LAJ, Wiegant JCAG, Vaandrager JW. Vrolijk J, den Dunnen J, Tanke HJ, van Ommen GJB (1996) Fiber-FISH as a DNA mapping tool. Methods Enzymol 9:67-73
Ried T, Baldini A, Rand TC, Ward DC (1992) Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and
digital imaging microscopy. Proc Nat! Acad Sci USA 89:1388-1392
Roberts I, Wienberg 1, Nacheva E, Grace C, Griffin D, Coleman N (1999) Novel method
for the production of multiple colour chromosome paints for use in karyotyping by
fluorescence in situ hybridisation. Genes Chromsom Cancer 25:241-250
Roux W (1883) Uber die Bedeutung der Kerntheilungsfiguren, Engelmann, Leipzig.
Rowley JD, Diaz MO, Espinosa R, Patel YD, van Melle E, Ziemin S, Taillon-Miller P et al
(1990) Mapping chromosome band llq23 in human acute leukemia with biotinylated probes: identification of 11q23 translocation breakpoints with a yeast artificial
chromosome. Proc Nat! Acad Sci USA 87:9358-9362
Rubin CM, Carrino JJ, Dickler MN, Leibowitz D, Smith SD, Westbrook CA (1988) Heterogeneity of genomic fusion of BCR and ABL in Philadelphia chromosome-positive
acute lymphoblastic leukemia. Proc Nat! Acad Sci USA 85:2795-2799
Saiki RK, Scharf S, Faloona F, Mullis KB, Horn GT, Erlich HA, Arnheim N (1985) Enzymatic amplification ofbeta-globin genomic sequences and restriction site analysis
for diagnosis of sickle cell anemia. Science 230:1350-1354
Schinzel A (1983) Catalog of unbalanced chromosome aberrations in man. Walter de
Gruyter and Co. Berlin, pp 1.7