An optimized probe set for the detection of small interchromosomal aberrations by use of 24-color FISH

American Journal of Human Genetics

Volumn 66, Issue 5, 2000, Pages 1684-1688

  Azofeifa, Jorge ^a,b   Fauth, Christine ^a   Kraus, Jürgen ^a   Maierhofer, Christine ^a   Langer, Sabine ^a   Bolzer, Andreas ^a   Reichman, Jay ^c   Schuffenhauer, Simone ^a   Speicher, Michael R ^a  

^a UNIVERSITY OF MUNICH   (Germany)

^b UNIVERSIDAD DE COSTA RICA   (Costa Rica)

^c Chroma Technology Corporation   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FLUOROCHROME;

ARTICLE; CHROMOSOME ABERRATION; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPING; PRIORITY JOURNAL;

EID: 0033926363     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302875     Document Type: Article

References (9)

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2. Haddad BR, Schröck E, Meek J, Cowan J, Young H, Ferguson-Smith MA, du Manoir S, et al (1998) Identification of de novo chromosomal markers and derivatives by spectral karyotyping. Hum Genet 103:619-625
3. Holinski-Feder E, Reyniers E, Uhrig S, Golla A, Wauters J, Kroisel P, Bossyut P, et al (2000) Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3). Am J Hum Genet 66: 16-25
4. Macville M, Schröck E, Padilla-Nash H, Keck C, Ghadimi BM, Zimonjic D, Popescu N, et al (1999) Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping. Cancer Res 59:141-150
5. National Institutes of Health and Institute of Molecular Medicine Collaboration (1996) A complete set of human telomeric probes and their clinical applications. Nat Genet 14: 86-89
6. Schröck E, du Manoir S, Veldman T, Schoell B, Wienberg J, Ferguson-Smith MA, Ning Y, et al (1996) Multicolor spectral karyotyping of human chromosomes. Science 273: 494-497
7. Schröck E, Veldman T, Padilla-Nash H, Ning Y, Spurbeck J, Jalal S, Shaffer LG, et al (1997) Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities. Hum Genet 101:255-262
8. Speicher MR, Gwyn Ballard S, Ward DC (1996) Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nat Genet 12:368-375
9. Uhrig S, Schuffenhauer S, Fauth C, Wirtz A, Daumer-Haas C, Apacik C, Cohen M, et al (1999) Multiplex-FISH (M-FISH) for pre-and postnatal diagnostic applications. Am J Hum Genet 65:448-462