Full Name
Shukarova Angelovska, Elena
Main Affiliation
 
Email
elena.shukarova.angelovska@medf.ukim.edu.mk
 
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Publications
(Articles)

Refined By:
Author:  Nestoroska, Dragica

Results 1-9 of 9 (Search time: 0.007 seconds).

PreviewTitleAuthor(s)Issue DateType
1Chromosomal abnormalities in couples that undergo assisted reproduction technologiesShukarova Angelovska, Elena ; Ilieva, Gordana; Anastasovska, Violeta ; Hristova-Dimkovska, Tanja; Nestoroska, Dragica17-Apr-2019Proceeding article
2Detection of 3p25 microdeletion syndrome in the Macedonian patient with significant psychomotor retardationAnastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Zdraveska, Nikolina ; Ilieva, Gordana; Pesevska, Milica; Stojanova, Ivana28-Aug-2021Proceeding article
3Detection of giant chromosomal material on 7p+ with conventional karyotyping and aCGHIlieva, Gordana; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Muaremoska-Kanzoska, Ljelja; Pesevska, Milica; Anastasovska, Violeta 28-Aug-2021Proceeding article
4Detection of the pathogenic CNVs in the Macedonian patient with profound developmental delayAnastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Zdraveska, Nikolina ; Ilieva, Gordana; Pesevska, Milica6-Jun-2020Proceeding article
5Development delay in paediatric patient with deletion on chromosome 15q26.2Pesevska, Milica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Ilieva, Gordana; Panovska, Sandra28-Aug-2021Proceeding article
6Duplication of 10q22.2q23.1 as a cause for severe hypotonia in a childIlieva, Gordana; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Naunova Timovska, Silvana ; Pesevska, Milica; Anastasovska, Violeta 6-Jun-2020Proceeding article
7Early onset of complex seizures as a first sign of 16p11.2 deletion syndromeShukarova Angelovska, Elena ; Anastasovska, Violeta ; Duma, Filip ; Muaremovska, Ljelja; Nestoroska, Dragica; Ilieva, Gordana; Pesevska, Milica; Velkov, Milan6-Jun-2020Proceeding article
8Genomic and clinical characterisation of microduplications in a patient with developmental delayNestoroska, Dragica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Pesevska, Milica; Ilieva, Gordana6-Jun-2020Proceeding article
9Paediatric patient with deletion on chromosome 10q11.22 diagnosed by aCGHPesevska, Milica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Ilieva, Gordana6-Jun-2020Proceeding article