Application of the cytogenetic techniques multiple FISH and multiple BAND. Report of five cases;Múltiple FISH y múltiple BAND: Técnicas de citogenética molecular en cinco casos

Revista Medica de Chile

Volumn 130, Issue 5, 2002, Pages 511-518

  Castillo Taucher, Silvia ^a   Fuentes S , Ana María ^c   Paulos M , Alejandro ^c   Pardo V , Andrea ^b  

^a UNIVERSIDAD DEL DESARROLLO   (Chile)

^b UNIVERSITY OF CHILE   (Chile)

^c Laboratorio Clínica Alemana ^*

Author keywords

Chromosome abnormalities; Cytogenetics; Neoplasms

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME ABERRATION; CHROMOSOME BANDING PATTERN; CHROMOSOME MAP; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HUMAN; INFANT; KARYOTYPING; MALE; METHODOLOGY; MIDDLE AGED; MYELOID LEUKEMIA; PRESCHOOL CHILD;

ADULT; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME MAPPING; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; LEUKEMIA, MYELOID; MALE; MIDDLE AGED;

EID: 0346678527     PISSN: 00349887     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (19)

1. TJIO JH, LEVAN A. The chromosome number of man. Hereditas 1956; 42: 1-6.
2. GRAY JW. Molecular cytogenetics: diagnostic and prognostic assessment. Curr Opin BiotecH 1992; 3: 623-31.
3. SCHRÖCK E, VELDMAN T, PADILLA-NASH H, NING Y, SPURBECK J, JALAL S ET AL. Spectral karyotyping refines cytogentic diagnostics of constitutional chromosomal abnormalities. Hum Genet 1997; 101: 255-62.
4. SPEICHER MR, GWYN BALLARD S, WARD DC. Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nature Genet 1996; 12: 368-75.
5. EILS R, UHRIG S, SARACOGLU K, SATZLER K, BOLZER A, PETERSEN I, CHASSERY J, GANSER M, SPEICHER MR. An optimized, fully automated system for fast and accurate identification of chromosomal rearrangements by multiplex FISH (M-FISH). Cytogenet Cell Genet 1998; 82: 160-71.
6. ROONEY DE, CZEPULKOWSKI BH. Human Cytogenetics: A practical approach Vol. 1 Oxford University Press, New York 1992.
7. MITELMAN F, ISCN. An International System for Human Cytogenetic Nomenclature. Ed. S Karger, Basel, 1995; 1-114.
8. Xcyte Laboratory Manual. Metasystems GmbH, Altlussheim, Germany. June, 2001.
9. LE BEAU MM. One FISH, two FISH, red FISH, blue FISH. Nature Genet 1996; 12: 341-4.
10. ROMANA SP, POIREL H, LECONIAT M, FLEXOR MA, MANCHAUFFE M, JOUVEAUX P, MACINTYRE EA, BERGER R, BERNARD OA. High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia. Blood 1995; 86: 4263-9.
11. BARCH M, KNUDSEN T, SPURBECK J. The AGT cytogenetics Laboratory Manual. Third Edition. Lippincott Raven, 1997; 325-72.
12. IDA T, HARADA N, ABE K, KANDOH T, YOSHINAGA M, MAKI T, NIIKAWA N. Identification of de novo chromosome rearrangements: Five cases with differential chromosome painting. Am J Med Genet 2002, published Online 17 January 2002, DO1 10.1002/amjg.10257, Forthcoming articles: articles available online in advance of print.
13. HARRISON CJ, GIBBONS B, YAMG F, BUTLER T, CHEUNG K, KEARNEY L ET AL. Multiplex Fluorescence In Situ Hybridization and Cross Species Color Banding of a Case of Chronic Myeloid Leukemia in Blastic Crisis with a Complex Philadelphia Translocation. Cancer Genet Cytogenet 2000; 116: 105-10.
14. UHRIG S, SCHUFFENHAUER A, FAUTH C, WIRTZ A, DAUMER HAAS C, APACIK C ET AL. Multiplex-FISH for Pre and Postnatal Diagnostic Applications. Am J Hum Genet 1997; 65: 448-62.
15. HADDAD BR, SCHRÖCK E, MECK J, COWAN J, YOUNG H. Identification of de novo chromosomal markers and derivatives by spectral karyotyping. Hum Genet 1998; 103: 619-25.
16. THILAGANATHAN B, SAIRAM S, BALLARD T, PETERSON C, MEREDITH R. Effectiveness of prenatal chromosomal analysis using multicolour fluorescent in situ hybridization. British Journal Obstetrics and Gynecology 2000; 107: 262-6.
17. LEE C, GISSELSSON D, JIN C, NORDGREN A, FERGUSON DO, BLENNOW E ET AL. Report: Limitations of Chromosoma Classification by Multicolor Karyotyping. Am J Hum Genet 2001; 68: 1043-7.
18. DU MANOIR S, SPEICHER MR, JOOS S, SCHROECK E, POPP S, DOEHNER H, KOVACS G, ROBERT-NICOUD M, LICHTER P, CREMER T. Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization. Hum Genet 1993; 90: 590-610.
19. BENQUIQUE OJOPI EP, ROGATTO SR, FÍGARO CALDEIRA JR, BARBIÉRI-NIETO J, SQUIRE JA. Comparative genomic hybridization detects novel amplifications in fibroadenomas of the breast. Genes Chromosomes Cancer 2001; 30: 25-31.