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Browsing by Author Kavečan, Ivana
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Issue Date | Title | Author(s) | Type | Мp-cat. |
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2016 | A case of 47,XYY in asscociation with congenital anomalies in teenage couple![]() | Kavečan, Ivana ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2016 | A case of craniorachischisis totalis![]() | Kavečan, Ivana ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2015 | A case of infant hot water epilepsy: A clinical commentary with video sequences | Redzek-Mudrinic, Tatjana B; Kavecan, Ivana I ![]() ![]() | Contribution to periodical | 22M22 |
2012 | Accessory Scrotum Attached to a Peduncular Perineal Lipoma | Kavecan, Ivana I ![]() ![]() | Article | 22M22 |
2021 | Analysis of mtDNA sequence in patients with mitochondriopathies![]() | Dawod, Phepy Gamal Amvar | Doctoral theses | 70M70 |
2017 | Approach to Pregnancy in Niemann Pick Disease Type B Patient![]() | Agic, Danijela D ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2021 | Assessment of intellectual impairment, health-related quality of life, and behavioral phenotype in patients with neurotransmitter related disorders: Data from the iNTD registry![]() | Keller, Mareike; ...; Kavecan, Ivana I ![]() ![]() | Article | 21M21 |
2009 | Autism and hypoplastic corpus callosum in a case of monocentric marker chromosome 15 | Jovanović Privrodski, Jadranka; Kavečan, Ivana ![]() ![]() | Article | 22M22 |
2021 | Birth of a healthy child fathered by a man with Klinefelter's syndrome after preimplantation genetic testing![]() | Trninic-Pjevic, Aleksandra M ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 23M23 |
2011 | CCFDN sindrom![]() | Radovanov, D; Jovanović-Privrodski, Jadranka ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2022 | Characteristics and quality of life of substance users and their caregivers![]() | Maksimovic, Jadranka M ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 21M21 |
2019 | Clinical and genetic aspects of overgrowth spectrum syndromes![]() | Kavečan, Ivana ![]() ![]() | Conference Paper | Mp. category will be shown later |
2023 | Clinical manifestations of Johanson-Blizzard syndrome in patient with nucleotide variants in UBR1 gene![]() | Jojkić-Pavkov, Danijela ![]() ![]() ![]() ![]() ![]() ![]() | Article | 23M23 |
2012 | Complete androgen insensitivity syndrome: Review of four cases | Dobanovacki, Dusanka; Jokić, Radoica ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | Mp. category will be shown later |
2022 | Could COVID19 cause hemifacial microsomia?![]() | Maksimović, Jadranka ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2008 | Deficit 21-hidroksilaze kao uzrok kongenitalne nadbubrežne hiperplazije : prikaz slučaja![]() | Vlaški, Jovan; Katanić, Dragan ![]() ![]() ![]() ![]() ![]() | Article | Mp. category will be shown later |
2022 | Detekcija i karakterizacija genomskih abnormalnosti kod novorođenčadi sa kritično teškim urođenim srčanim manama | Miletić, Aleksandra | Doctoral theses | 70M70 |
2018 | Duchenne and Becker Muscular Dystrophy and Epilepsy | Redzek-Mudrinic, Tatjana B; Kavecan, Ivana I ![]() ![]() | Conference Paper | Mp. category will be shown later |
2017 | Early recurrent pregnancy lost caused by paternal translocation t(3;8)(q13;q24)![]() | Kavečan, Ivana ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2015 | Epigenetika![]() | Kavečan, Ivana ![]() ![]() ![]() | Article | 52M52 |