Pregled bibliografske jedinice broj: 73918
Application of fluorescence in situ hybridization (FISH) in clinical genetics
Application of fluorescence in situ hybridization (FISH) in clinical genetics // Paediatria Croatica, 45 (2001), 4; 175-178 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 73918 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Application of fluorescence in situ hybridization (FISH) in clinical genetics
(Application of flurescence in situ hybridization (FISH) in clinical genetics)
Autori
Petković, Iskra ; Barišić, Ingeborg
Izvornik
Paediatria Croatica (1330-1403) 45
(2001), 4;
175-178
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
chromosome aberrations; cytogenetics- methods; in situ hybridiszation; fluorescence
Sažetak
In this paper we present the results of cytogenetic and FISH analysis in 20 patients referred for suspected constitutional chromosomal aberrations. The aim of this report is to evaluate the advantages and limitations of routine karyotyping and the FISH method in the detection of various types of genome rearrangements. This study demonstrates a number of advantages of the FISH method over conventional cytogenetic such as the possibility of investigating genomic imbalance in non-dividing cells, the detection of cytogenetically invisible microdeletions and distinction of intra-from interchromosomal rearrangements. The FISH method, however, presents some limitations such as the impossibility of simultaneous detection and identification of every chromosome in a metaphase spread and precise identification of the chromosomal segment involved in duplications, inversions or deletions.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti, Javno zdravstvo i zdravstvena zaštita
Citiraj ovu publikaciju:
Časopis indeksira:
- Scopus
Uključenost u ostale bibliografske baze podataka::
- Excerpta Medica