Interstitial 14q31.3-q32.13 deletion
Aim: With the exception of ring chromosome 14 or translocations, interstitial deletions of the long arm of chromosome 14 are very rare. All patients with these deletions share common phenotypic characteristics, primarily mild dysmorphia and developmental delay. Molecular karyotyping (array CGH) enab...
| Permalink: | http://skupni.nsk.hr/Record/nsk.NSK01001079626/Similar |
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| Matična publikacija: |
Molecular and experimental biology in medicine 2 (2019), 1 ; str. 48-51 |
| Glavni autori: | Crkvenac Gornik, Kristina (Author), Tonković, Ivana, liječnica, Pokupec Bilić, Anita, Huljev Frković, Sanda |
| Vrsta građe: | e-članak |
| Jezik: | eng |
| Predmet: | |
| Online pristup: |
Elektronička verzija članka Elektronička verzija članka Hrčak |
APA stil citiranja
Crkvenac Gornik, K. (2019). Interstitial 14q31.3-q32.13 deletion: Interstitial 14q31.3-q32.13 deletion [Elektronička građa] : the role of molecular karyotyping in clarifying the etiology of developmental delay. Molecular and experimental biology in medicine.
Chicago stil citiranjaCrkvenac Gornik, Kristina. "Interstitial 14q31.3-q32.13 deletion: Interstitial 14q31.3-q32.13 deletion [Elektronička građa] : the role of molecular karyotyping in clarifying the etiology of developmental delay." 2019.
MLA stil citiranjaCrkvenac Gornik, Kristina. "Interstitial 14q31.3-q32.13 deletion: Interstitial 14q31.3-q32.13 deletion [Elektronička građa] : the role of molecular karyotyping in clarifying the etiology of developmental delay." 2019.