Pregled bibliografske jedinice broj: 423241
De novo balanced translocation t(18 ; 20)(q21.3 ; q12) in a mentally retarded girl
De novo balanced translocation t(18 ; 20)(q21.3 ; q12) in a mentally retarded girl // Chromosome Research / Macgregor, Herbert (ur.).
Stockholm, Švedska: Springer, 2009. str. 49-49 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 423241 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
De novo balanced translocation t(18 ; 20)(q21.3 ; q12) in a mentally retarded girl
Autori
Vraneković, Jadranka ; Brajenović-Milić, Bojana ; Babić-Božović, Ivana ; Peterlin, Borut ; Kapović, Miljenko ; Riegel, Mariluce
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Chromosome Research
/ Macgregor, Herbert - : Springer, 2009, 49-49
Skup
Seventh European Cytogenetics Conference
Mjesto i datum
Stockholm, Švedska, 04.07.2009. - 07.07.2009
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
De novo balanced translocation; mental retardation
Sažetak
We report a twenty-year-old girl with mental retardation, obesity, hirsutism and de novo balanced t(18 ; 20)(q21.3 ; q12) translocation. Fluorescence in situ hybridization (FISH) using whole chromosome paint probe 18, the partial chromosome paint 20 (PCP RH17J3), RP11-15C15C (18q21.32-33) and YAC942B1 (20q12) clones were used to precisely define the translocation breakpoints. Based on GTG-banding and FISH analyses, the patient’ s karyotype was interpreted as: 46, XX, t(18 ; 20)(q21.3 ; q12)[20].isht(18 ; 20)(YAC-942B1+ ; RP11-15C15+)[20]de novo. Aarray-comparative genomic hybridisation (a-CGH) examination using 44k and 244A (Agilent) oligonucleotide arrays did not detect a deletion or duplication, neither at the breakpoints or elsewhere in the genome. The abnormal phenotype observed in the patient could be explained by gene disruption, a position effect or could have occurred by coincidence.
Izvorni jezik
Engleski
POVEZANOST RADA
Projekti:
062-0000000-1349 - Prenatalni probir za sindrom Downov (Brajenović-Milić, Bojana, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Rijeka
Profili:
Bojana Brajenović-Milić
(autor)
Ivana Babić Božović
(autor)
Miljenko Kapović
(autor)
Jadranka Vraneković
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE