izvor podataka: crosbi
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Phenotype Application of Flourescence In Situ Hybridization in Cytogenetic Syndromes (CROSBI ID 85222)
Prilog u časopisu | izvorni znanstveni rad
Begović, Davor ; Hitrec, Vlasta ; Lasan, Ružica ; Letica, Ljiljana ; Barić, Ivo ; Sarnavka, Vladimir ; Galić, Slobodan
Phenotype Application of Flourescence In Situ Hybridization in Cytogenetic Syndromes // Croatian medical journal, 39 (1998), 2; 212-215-x
Podaci o odgovornosti
Begović, Davor ; Hitrec, Vlasta ; Lasan, Ružica ; Letica, Ljiljana ; Barić, Ivo ; Sarnavka, Vladimir ; Galić, Slobodan
engleski
Phenotype Application of Flourescence In Situ Hybridization in Cytogenetic Syndromes
We report on a month-old infant with dysmorphic face and several anomalies known to be associated with trisomy 13. Fluorescence in situ hybridization studies performed on metaphase cells allowed us to identify an extra material on the short arm of the chromosome 13 as a duplication of 13q22-qter
aneuploidy;banding chromosome;cytogenetics;FISH;trisomy 13
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