42
EIGIL KJELDSEN and STEEN K0LVRAA
Christian AT, Garcia HE, Tucker JD (1999) PCR in situ followed by microdissection
allows whole chromosome painting probes to be made from single microdissected
chromosomes. Mamm Genome 10:628-631
Chudoba I, Plesch A, Lorch T, Lemke J, Claussen U, Senger G (1999) High resolution
multicolor-banding: a new technique for refined FISH analysis of human chromosomes. Cytogenet Cell Genet 84:156-160
Choo KHA (1994) Methods in Molecular Biology, Vol. 33: In situ hybridization Protocols. Humana Press Inc., Totowa, NJ
Cohen SN, Chang ACY, Boyer HW, Helling RB (1973) Construction of biologically
functional bacterial plasmids in vitro. Proc Nat! Acad Sci USA 70:3240-3244
Craig JM, Kraus J, Cremer T (1997) Removal of repetitive sequences from FISH probes
using PCR-assisted affinity chromatography. Hum Genet 100:472-476
Cremer T, Landegent J, Bruckner A, Scholl HP, Schardin M, Hager HD, Devilee P,
Pearson P, van der Ploeg M (1986) Detection of chromosome aberrations in the
human interphase nucleus by visualization of specific target DNAs with radioactive
and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with
probe L1.84. Hum Genet 74:346-352
Cremer T, Lichter P,Borden J, Ward DC, Manuelidis L (1988) Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization
using chromosome specific library probes. Hum Genet 80:235-246
Daubendiek SL and Kool ET (1997) Generation of catalytic RNAs by rolling transcription of synthetic DNA nanocircles. Nature Biotech 15:273-277
Deaven LL, Van Dilla MA, Bartholdi MF, Carrano AV, Cram LS, Fuscoe JC, Gray JW,
Hildebrand CE, Moyzis RK, Perlman J (1986) Construction of human chromosomespecific DNA libraries from flow-sorted chromosomes. Cold Spring Harb Symp
Quant BioI 51:159-167
DeIhanty JDA, Griffin DK, Handyside AH, Harper J, Atkinson GHG, Pieters MHEC,
Winston RML (1993) Detection of aneuploidy and chromosomal mosaicism in human embryos during preimplantation sex determination by fluorescent in situ hybridization, (FISH). Hum Mol Genet 2:1183-1185
Dobyns WB, Curry CTR, Hoyme HE, Turlington L, Ledbetter DH (1991) Clinical and
molecular diagnosis of Miller-Dieker syndrome. Am J Hum Genet 48:584-594
duManoirS,SpeicherMR,JoosS, SchrockE,PoppS, DohnerH,KovacsG,Robert-Nicoud
M,LichterP,CremerT(1993) Detectionofcomplete and partial chromosome gains and
losses by comparative genomic hybridization. Hum Genet 90:590-610
Edwards JH, Harnden DG, Cameron AH, Crosse VM, WolffOH (1960) A new trisomic
syndrome. Lancet 1:787-790
Egholm M, Buchardt 0, Christensen L, Behrens C, Freier S, Driver DA, Berg RH, Kim
SK, Norden B, Nielsen PE (1993) PNA hybridizes to complementary oligonucleotides obeying the Watson-Crick hydrogen bonding rules. Nature 365:566-568
Flemming W (1882) Zellsubstanz, Kern und Zellteilung. Leipzig.
Flint J, Wilkie AOM, Buckle VJ, Winter RM, Holland AJ, McDermid HE (1995) The
detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation. Nat Genet 9:132-140
Florijn RJ, van de Rijke FM, Vrolijk J, Blonden LAJ, Hotker MH, den Dunnen JT, Tanke
HI, van Ommen GJB, Raap AK (1996) Exon mapping by fiber-FISH or LR-PCR.
Genomics 38:277-282
Ford CE, Jacobs PA, Lajtha LG (1958) Human somatic chromosomes. Nature, London;
181:1565-1568
EIGIL KJELDSEN and STEEN K0LVRAA
Christian AT, Garcia HE, Tucker JD (1999) PCR in situ followed by microdissection
allows whole chromosome painting probes to be made from single microdissected
chromosomes. Mamm Genome 10:628-631
Chudoba I, Plesch A, Lorch T, Lemke J, Claussen U, Senger G (1999) High resolution
multicolor-banding: a new technique for refined FISH analysis of human chromosomes. Cytogenet Cell Genet 84:156-160
Choo KHA (1994) Methods in Molecular Biology, Vol. 33: In situ hybridization Protocols. Humana Press Inc., Totowa, NJ
Cohen SN, Chang ACY, Boyer HW, Helling RB (1973) Construction of biologically
functional bacterial plasmids in vitro. Proc Nat! Acad Sci USA 70:3240-3244
Craig JM, Kraus J, Cremer T (1997) Removal of repetitive sequences from FISH probes
using PCR-assisted affinity chromatography. Hum Genet 100:472-476
Cremer T, Landegent J, Bruckner A, Scholl HP, Schardin M, Hager HD, Devilee P,
Pearson P, van der Ploeg M (1986) Detection of chromosome aberrations in the
human interphase nucleus by visualization of specific target DNAs with radioactive
and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with
probe L1.84. Hum Genet 74:346-352
Cremer T, Lichter P,Borden J, Ward DC, Manuelidis L (1988) Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization
using chromosome specific library probes. Hum Genet 80:235-246
Daubendiek SL and Kool ET (1997) Generation of catalytic RNAs by rolling transcription of synthetic DNA nanocircles. Nature Biotech 15:273-277
Deaven LL, Van Dilla MA, Bartholdi MF, Carrano AV, Cram LS, Fuscoe JC, Gray JW,
Hildebrand CE, Moyzis RK, Perlman J (1986) Construction of human chromosomespecific DNA libraries from flow-sorted chromosomes. Cold Spring Harb Symp
Quant BioI 51:159-167
DeIhanty JDA, Griffin DK, Handyside AH, Harper J, Atkinson GHG, Pieters MHEC,
Winston RML (1993) Detection of aneuploidy and chromosomal mosaicism in human embryos during preimplantation sex determination by fluorescent in situ hybridization, (FISH). Hum Mol Genet 2:1183-1185
Dobyns WB, Curry CTR, Hoyme HE, Turlington L, Ledbetter DH (1991) Clinical and
molecular diagnosis of Miller-Dieker syndrome. Am J Hum Genet 48:584-594
duManoirS,SpeicherMR,JoosS, SchrockE,PoppS, DohnerH,KovacsG,Robert-Nicoud
M,LichterP,CremerT(1993) Detectionofcomplete and partial chromosome gains and
losses by comparative genomic hybridization. Hum Genet 90:590-610
Edwards JH, Harnden DG, Cameron AH, Crosse VM, WolffOH (1960) A new trisomic
syndrome. Lancet 1:787-790
Egholm M, Buchardt 0, Christensen L, Behrens C, Freier S, Driver DA, Berg RH, Kim
SK, Norden B, Nielsen PE (1993) PNA hybridizes to complementary oligonucleotides obeying the Watson-Crick hydrogen bonding rules. Nature 365:566-568
Flemming W (1882) Zellsubstanz, Kern und Zellteilung. Leipzig.
Flint J, Wilkie AOM, Buckle VJ, Winter RM, Holland AJ, McDermid HE (1995) The
detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation. Nat Genet 9:132-140
Florijn RJ, van de Rijke FM, Vrolijk J, Blonden LAJ, Hotker MH, den Dunnen JT, Tanke
HI, van Ommen GJB, Raap AK (1996) Exon mapping by fiber-FISH or LR-PCR.
Genomics 38:277-282
Ford CE, Jacobs PA, Lajtha LG (1958) Human somatic chromosomes. Nature, London;
181:1565-1568