Bifid cardiac apex in Pallister-Killian syndrome
Aim: Pallister-Killian syndrome (PKS) is a rare chromosomal disorder, caused by tissue-limited mosaicism for an isochromosome 12p. Prenatal diagnosis of PKS is generally incidental. Although clinical presentation of PKS varies, cytogenetic findings are constant, and include a tetrasomy of chromosome...
| Permalink: | http://skupnikatalog.nsk.hr/Record/nsk.NSK01001098397 |
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| Matična publikacija: |
Medicina Fluminensis (Online) 56 (2020), 2 ; str. 189-192 |
| Glavni autori: | Barišić, Anita (Author), Finderle, Aleks, Petrović, Oleg, liječnik, Vraneković, Jadranka |
| Vrsta građe: | e-članak |
| Jezik: | eng |
| Predmet: | |
| Online pristup: |
https://doi.org/10.21860/medflum2020_237307 Hrčak |