1 FISH Techniques, FISH Probes and Their Applications in Medicine and Biology - An Overview
43
Ford CE, Jones KW, Polani PE, Almeida JCDE, Briggs JH (1959) A sex-chromosomal
anomaly in a case of gonadal dysgenesis (Turner's syndrome). Lancet 1:711-713
Gerhard DS, Kawasaki ES, Bancroft FC, Szabo P (1981) Localization of a unique gene by
direct hybridization in situ. Proc Natl Acad Sci USA 78:3755-3759
Gilmore JH, Lawler CP, Eaton AM, Mailman RB (1993) Postmortem stability of dopamine Dl receptor mRNA and Dl receptors. Brain Res Mol Brain Res 18:290-296
Giraudeau F, Aubert D, Young I, Horsley S, Knight S, Kearney L, Vergnaud G, Flint J
(1997) Molecular cytogenetic detection of a deletion of Ip36.3. J Med Genet 34:314317
Goldman ASH, Hulten MA (1992) Chromosomes in situ suppression hybridization in
human male meiosis. J Med Genet 29:98-102
Goodwin EH, Meyne J, Bailey SM Quigley D (1996) On the origin oflateral assymetry.
Chromosoma 104:345-347
Gosden J, Hanratty D, Starling J, Fantes J, Mitchell A, Porteus D (1991) Oligonucleotide-primed in situ DNA synthesis (PRINS): a method for chromosome mapping.
banding, and investigation of sequence organization. Cytogenet Cell Genet 57:100104
Guan X-Y, Trent JM, Meltzer PS (1993) Generation of band-specific painting probes
from a single microdissected chromosome. Hum Mol Genet 2:1117-1121
Guan X- Y, Zhang H, Bittner M, Jiang Y, Meltzer PS, Trent JM (1996) Chromosome arm
painting probes. Nat Genet 12:10-12
HaafT and Ward DC (1994) High resolution ordering ofYAC contigs using extended
chromatin and chromosomes. Hum Mol Genet 3:629-633
Hachitanda Y, Saito M, Mori T, Hamazaki M (1997) Application of fluorescence in situ
hybridization to detect N-myc (MYCN) gene amplification on paraffin-embedded
tissue sections of neuroblastomas Med Pediatr Oncol 2:135-138
Harper M & Saunders G (1981) Localization of single copy DNA sequences on Gbanded human chromosomes by in situ hybridization. Chromosoma 83:431-439
Heiskanen M, Peltonen L, Palotie A (1996) Visual mapping by high resolution FISH.
Trends Genet 12:379-382
Heng HHQ, Squire J, Tsui LC (1992) High resolution mapping of mammalian genes by
in situ hybridization to free chromatin. Proc Natl Acad Sci USA 89:9509-9513
Hindkjrer 1, Koch J, Mogensen J, K01vraa S, Bolund (1994) Primed InSitu (PRINS) labeling of DNA. In: Choo KHA (ed.) In situ hybridization Protocols. Methods in
Molecular Biology. vol 33. Humana Press Inc., Totowa, NJ, pp 95-107
Hsu TC (1952) Mammalian chromosomes in vitro. I. The karyotype of man. J Hered
43:167-172
Hulten MA, Gould CP, Goldman ASH, Waters JJ (1991) Chromosome in situ suppression hybridization in clinical cytogenetics. J Med Genet 28:577-582
Iida S, Rao PH, Butler M, Corradini P, Boccadoro M, Klein B, Chaganti RS, Dalla-Favera R (1997) Deregulation of MUM l/IRF4 by chromosomal translocation in multiple myeloma. Nat Genet 17:226-230
Kallioniemi A, Kallioniemi O-P, Sudar D, Rutovitz D, Gray JW, Waldman F, Pinkel D
(1992) Comparative genomic hybridization for molecular cytogentic analysis of solid tumours. Science 258:818-821
Kalousek DK, Langlois S, Robinson WP, Telenius A, Bernard L, Barrett IJ, HowardPeebles PN, Wilson RD (1996) Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases. Am J Med Genet 65:348-352
43
Ford CE, Jones KW, Polani PE, Almeida JCDE, Briggs JH (1959) A sex-chromosomal
anomaly in a case of gonadal dysgenesis (Turner's syndrome). Lancet 1:711-713
Gerhard DS, Kawasaki ES, Bancroft FC, Szabo P (1981) Localization of a unique gene by
direct hybridization in situ. Proc Natl Acad Sci USA 78:3755-3759
Gilmore JH, Lawler CP, Eaton AM, Mailman RB (1993) Postmortem stability of dopamine Dl receptor mRNA and Dl receptors. Brain Res Mol Brain Res 18:290-296
Giraudeau F, Aubert D, Young I, Horsley S, Knight S, Kearney L, Vergnaud G, Flint J
(1997) Molecular cytogenetic detection of a deletion of Ip36.3. J Med Genet 34:314317
Goldman ASH, Hulten MA (1992) Chromosomes in situ suppression hybridization in
human male meiosis. J Med Genet 29:98-102
Goodwin EH, Meyne J, Bailey SM Quigley D (1996) On the origin oflateral assymetry.
Chromosoma 104:345-347
Gosden J, Hanratty D, Starling J, Fantes J, Mitchell A, Porteus D (1991) Oligonucleotide-primed in situ DNA synthesis (PRINS): a method for chromosome mapping.
banding, and investigation of sequence organization. Cytogenet Cell Genet 57:100104
Guan X-Y, Trent JM, Meltzer PS (1993) Generation of band-specific painting probes
from a single microdissected chromosome. Hum Mol Genet 2:1117-1121
Guan X- Y, Zhang H, Bittner M, Jiang Y, Meltzer PS, Trent JM (1996) Chromosome arm
painting probes. Nat Genet 12:10-12
HaafT and Ward DC (1994) High resolution ordering ofYAC contigs using extended
chromatin and chromosomes. Hum Mol Genet 3:629-633
Hachitanda Y, Saito M, Mori T, Hamazaki M (1997) Application of fluorescence in situ
hybridization to detect N-myc (MYCN) gene amplification on paraffin-embedded
tissue sections of neuroblastomas Med Pediatr Oncol 2:135-138
Harper M & Saunders G (1981) Localization of single copy DNA sequences on Gbanded human chromosomes by in situ hybridization. Chromosoma 83:431-439
Heiskanen M, Peltonen L, Palotie A (1996) Visual mapping by high resolution FISH.
Trends Genet 12:379-382
Heng HHQ, Squire J, Tsui LC (1992) High resolution mapping of mammalian genes by
in situ hybridization to free chromatin. Proc Natl Acad Sci USA 89:9509-9513
Hindkjrer 1, Koch J, Mogensen J, K01vraa S, Bolund (1994) Primed InSitu (PRINS) labeling of DNA. In: Choo KHA (ed.) In situ hybridization Protocols. Methods in
Molecular Biology. vol 33. Humana Press Inc., Totowa, NJ, pp 95-107
Hsu TC (1952) Mammalian chromosomes in vitro. I. The karyotype of man. J Hered
43:167-172
Hulten MA, Gould CP, Goldman ASH, Waters JJ (1991) Chromosome in situ suppression hybridization in clinical cytogenetics. J Med Genet 28:577-582
Iida S, Rao PH, Butler M, Corradini P, Boccadoro M, Klein B, Chaganti RS, Dalla-Favera R (1997) Deregulation of MUM l/IRF4 by chromosomal translocation in multiple myeloma. Nat Genet 17:226-230
Kallioniemi A, Kallioniemi O-P, Sudar D, Rutovitz D, Gray JW, Waldman F, Pinkel D
(1992) Comparative genomic hybridization for molecular cytogentic analysis of solid tumours. Science 258:818-821
Kalousek DK, Langlois S, Robinson WP, Telenius A, Bernard L, Barrett IJ, HowardPeebles PN, Wilson RD (1996) Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases. Am J Med Genet 65:348-352