A fast, novel approach for DNA fibre-fluorescence in situ hybridization analysis

Chromosome Research

Volumn 5, Issue 2, 1997, Pages 145-147

  Mann, Suzanne M ^a   Burkin, Dean J ^a,b   Grin, Darren K ^a   Ferguson Smith, Malcolm A ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b UNIVERSITY OF OTAGO   (New Zealand)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME; DNA HYBRIDIZATION; FLUORESCENCE IN SITU HYBRIDIZATION; PRIORITY JOURNAL;

EID: 0030932647     PISSN: 09673849     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1018426426477     Document Type: Article

References (5)

1. Carter NP, Ferguson-Smith MA, Perryman MT, Telenius H, Pelmear AH, Leversha MA, Glancy MT, Wood SL, Cook K, Dyson HM, Ferguson-Smith ME, Willatt LR (1992) Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics. J Med Genet 29: 299-307.
2. Fidlerová H, Senger G, Kost M, Sanseau P, Sheer D (1994) Two simple procedures for releasing chromatin from routinely fixed cells for fluorescence in situ hybridisation. Cytogenet Cell Genet 65: 203-205.
3. Heiskanen M, Karhu R, Hellsten E, Peltonen L, Kallioniemi OP, Palotie A (1994) High resolution mapping using fluorescence in situ hybridisation to extended chromatin fibers prepared from agarose-embedded cells. Biotechniques 17: 928-933.
4. Wiegant J, Kalle W, Mullenders L, Brookes S, Hoovers JMN, Dauwerse JG, van Ommen GJB, Raap AK (1992) Highresolution in situ hybridization using DNA halo preparations. Hum Mol Genet 1: 587-591.
5. Zheng YL, Ferguson-Smith MA, Warner JP, Ferguson-Smith ME, Sargent CA, Carter NP (1992) Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contig. Prenatal Diagnosis 12: 931-943.