1. Lebo RV, Flandermeyer RR, Diukman R, Lynch ED, Leperrcq JA, Golbus MS. Prenatal diagnosis with repetitive in situ hybridization probes. Am J Med Genet 1992; 43(5): 848-854.
2. Eastmond DA, Schuler M, Rupa DS. Advantages and limitations of using fluorescence in situ hybridization for the detection of aneuploidy in interphase human cells. Mutat Res 1995; 348(4): 153-162.
3. Koch JE, Kolvraa S, Petersen KB, Gregersen N, Bolund L. Oligonucleotide-priming methods for the chromosome-specific labeling of alpha satellite DNA in situ. Chromosoma 1989; 98(4): 259-265.
4. Bottema CDK, Sommer SS. PCR amplification of specific alleles: rapid detection of known mutations and polymorphisms. Mutat Res 1993; 288(1): 93-102.
5. Pellestor F, Girardet A, Andréo B, Charlieu JP. A polymorphic alpha satellite sequence specific for human chromosome 13 detected by oligonucleotide primed in situ labeling (PRINS). Hum Genet 1994; 94(4): 346-348.
6. Gosden J, Lawson D. Rapid chromosome identification by oligonucleotide-primed in situ DNA synthesis (PRINS). Hum Mol Genet 1994; 3(6): 931-936.
7. Hindkjaer J, Koch, J, Terkelsen C, Brandt CA, Kolvraa S, Bolund L. Fast, sensitive multicolor detection of nucleic acids in situ by primed in situ labeling (PRINS). Cytogenet Cell Genet 1994; 66(3): 152-154.
8. Yan L, Bronsard M, Drouin R. Creating a new color by omission of 3’ end blocking step for simultaneous detection of different chromosomes in multi-PRINS technique. Chromosoma 2001; 109(8): 565-570.
9. Kipling D, Wilson HE, Mitchell AR, Taylor BA, Cooke HJ. Mouse centromere mapping using oligonucleotide probes that detect variants of the minor satellite. Chromosoma 1994;103(1): 46-55.
10. Russo A, Priante G, Tommasi AM: PRINS localization of centromeres and telomeres in micronuclei indicates that in mouse splenocytes chromatid non-disjunction is a major mechanism of aneuploidy. Mutat Res 1996; 372(2):173-180.
11. Martins C, Galetti PM. Chromosomal localization of 5S rDNA genes in Leporinus fish (Anostomidae, Characiformes). Chromosome Res 1999; 7(5): 363-367.
12. Gu HF, Lind MI, Wieslander L, Landegren U, Söderhäll K, Melefors O. Using PRINS for gene mapping in polytene chromosomes. Chromosome Res 1997; 5(7): 463-465.
13. Pich U, Meister A, Macas J, Dolezel J, Lucretti S, Schubert I. Primed in situ labeling facilitates flow sorting of similar sized chromosomes. Plant J 1995; 7: 1039-1044.
14. Abbo S, Dunford RP, Miller TE, Reader SM, King IP. Primer-mediated in situ detection of the B-hordein gene cluster on barley chromosome 1H. Proc Natl Acad Sci USA 1993; 90(24): 11821-11824.
15. Pellestor F, Girardet A, Lefort G, Andréo B, Charlieu JP. Selection of chromosome-specific primer and their use in simple and double PRINS techniques for rapid in situ identification of human chromosomes. Cytogenet Cell Genet 1995;70(1-2): 138-142.
16. Velagelati, GVN, Shulman LP, Phillips OP, Tharapel SA, Tharapel AT. Primed in situ labeling for rapid prenatal diagnosis. Am J Obstet Gynecol 1998; 178(6): 1313-1320.
17. Pellestor F, Girardet A, Andréo B, Lefort G, Charlieu JP. Preimplantation embryo chromosome analysis by primed in situ labeling method. Fertil Steril 1996; 66(5): 781-786.
18. Findlay I, Corby N, Rutherford A, Quirke P. Comparison of FISH, PRINS, and conventional and fluorescent PCR for single-cell sexing; suitability for preimplantation genetic diagnosis. J Assist Reprod Genet 1998; 15(5): 258-265.
19. Hindkjaer J, Hammoudah SAFM, Hansen KB, Jensen PD, Koch J, Pedersen B. Translocation (1;16) identified by chromosome painting and primed in situ labeling (PRINS). Cancer Genet Cytogenet 1995; 79(1): 15-20.
20. Callen DF, Yip MY, Eyre HJ. Rapid detection of euchromatin by Alu-PRINS: use in clinical cytogenetics. Chromosome Res 1997; 5(2): 81-85.
21. Orsetti B, Lefort G, Boulot P, Andréo B, Pellestor F. Fetal cells in maternal blood: the use of primed in situ (PRINS) labelling technique for fetal cell detection and sex assessment. Prenat Diagn 1998; 18(10): 1014-1022.
22. Pellestor F, Girardet A, Coignet L, Andréo B, Charlieu JP. Assessment of aneuploidy for chromosomes 8, 9, 13, 16 and 21 in human sperm by using primed in situ labeling technique. Am J Hum Genet 1996; 58(4): 797-802.
23. Pellestor F, Girardet A, Andréo B, Lefort G, Charlieu JP. Incidence of chromosome 1 disomy in human sperm estimated by the primed in situ (PRINS) labelling technique. Cytogenet Cell Genet 1997; 76(3-4): 192-195.
24. Troyer DL, Xie H, Goad DW, Skinner DZ. Use of a new technique to map the porcine alpha interferon gene to chromosome 1. Mamm Genome 1994; 5(2): 112-114.
25. Kadandale J, Wachtel SS, Tunca Y, Wilroy RS, Martens PR, Tharapel AT. Localization of SRY by primed in situ labeling in XX and XY sex reversal. Am J Med Genet 2000; 95(1): 71-74.
26. Nielsen PE, Egholm M, Berg RH, Buchardt O. Sequence-selective recognition of DNA by strand displacement with a thymine-substituted polyamide. Science 1991; 254(5037): 1497-1500.
27. Corey DR. Peptide nucleic acids: expanding the scope of nucleic acid recognition. Trends BioTechnol 1997; 15(6): 224-229.
28. Von Wintzingerode F, Landt O, Ehrlich A, Gobel UB. Peptide nucleic acid-mediated PCR clamping as a useful supplement in the determination of microbial diversity. Appl Environ Microbiol 2000; 66(2): 549-557.
29. Larsen HJ, Bentin T, Nielsen PE. Antisense properties of peptide nucleic acid. Biochim Biophys Acta 1999; 1489(1): 159-166.
30. Lansdorp PM, Verwoerd NP, van de Rijke FM, Dragowska V, Little MT, Dirks RW, Raap AK, Tanke HJ. Heterogeneity in telomere length of human chromosomes. Hum Mol Genet 1996; 5(5): 685-691.
31. Taneja KL. Localization of trinucleotide repeat sequences in myotonic dystrophy cells using a single fluorochrome-labeled PNA probe. BioTechniques 1998; 24(3): 472-476.
32. Chen C, Hong YK, Ontiveros SD, Egholm M, Strauss WM: Single base discrimination of CENP-B repeats on mouse and human chromosomes with PNA-FISH. Mamm Genome 1999; 10(1): 13-18.
33. Chen C, Wu B, Wei T, Egholm M, Strauss WM. Unique chromosome identification and sequence-specific structural analysis with short PNA oligomers. Mamm Genome 2000; 11(5): 384-391.
34. Taneja KL, Chavez EA, Coull J, Lansdorp PM. Multicolor fluorescence in situ hybridization with peptide nucleic acid probes for enumeration of specific chromosomes in human cells. Genes Chromosomes Cancer 2001; 30(1): 57-63.
35. Pellestor F, Andréo B, Taneja K, Williams B. PNA on human sperm: a new approach for in situ aneuploidy estimation. Eur J Hum Genet 2003; 11(4): 337-341.