Zobrazeno 1 - 10 of 76 pro vyhledávání: '"Zagorac, Andreja"'
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Akademický článek
Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report
Autor: Zagorac Andreja, Marcun Varda Natasa, Krgovic Danijela, Kokalj-Vokac Nadja
Publikováno v: Molecular Cytogenetics, Vol 4, Iss 1, p 17 (2011)
Abstract Background Except for terminal deletions that lead to Jacobsen syndrome, interstitial deletions involving the long arm of chromosome 11 are not frequently reported. A clinically distinct phenotype is usually observed in these cases, and no c
Externí odkaz: https://doaj.org/article/33a6df0484dc4552b5b67418ef13dd3c
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5
Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report
Autor: Krgović, Danijela, Marčun-Varda, Nataša, Zagorac, Andreja, Kokalj-Vokač, Nadja
Publikováno v: Molecular Cytogenetics, vol. 4, pp. 1-17, 2011.
Background: Except for terminal deletions that lead to Jacobsen syndrome, interstitial deletions involving the long arm of chromosome 11 are not frequently reported. A clinically distinct phenotype is usually observed in these cases, and no clear gen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1857::7561c965233bcd5e7c6115d16295cf2c
https://dk.um.si/Dokument.php?id=113349&dn=
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6
An evaluation of SOX2 and hTERC gene amplifications as screening markers in oral and oropharyngeal squamous cell carcinomas
Autor: Kokalj-Vokač, Nadja, Čizmarevič, Bogdan, Zagorac, Andreja, Zagradišnik, Boris, Lanišnik, Boštjan
Publikováno v: Molecular Cytogenetics, vol. 7, pp. 1-8.
Background: Oral and oropharyngeal squamous cell carcinomas (OSCC) are among the most common cancers. The poor survival rate among oral cancer patients can be attributed to several factors, one of them being lack of early detection. A key approach to
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1857::1feeb55bf52d2973b54d268962ce00cc
https://plus.si.cobiss.net/opac7/bib/4897599?lang=sl
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7
TMPRSS2:ERG gene aberrations may provide insight into pT stage in prostate cancer
Autor: Krstanoski, Zoran, Kokalj-Vokač, Nadja, Zagorac, Andreja, Pospihalj, Boris, Munda, Miha, Džeroski, Sašo, Golouh, Rastko
Publikováno v: BMC Urology, vol. 16, pp. 1-6, 2016.
Background: TMPRSS2:ERG gene aberration may be a novel marker that improves risk stratification of prostate cancer before definitive cancer therapy, but studies have been inconclusive. Methods: The study cohort consisted of 202 operable prostate canc
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1857::eb039f3e909b4a0625a0105a56a9de34
https://plus.si.cobiss.net/opac7/bib/29626407?lang=sl
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8
A coalescence of two syndromes in a girl with terminal deletion and inverted duplication of chromosome 5
Autor: Krgović, Danijela, Blatnik, Ana, Burmas, Ante, Zagorac, Andreja, Kokalj-Vokač, Nadja
Publikováno v: BMC Medical Genetics, vol. 15, pp. 1-9, 2014.
Background: Rearrangements involving chromosome 5p often result in two syndromes, Cri-du-chat (CdC) and Trisomy 5p, caused by a deletion and duplication, respectively. The 5p15.2 has been defined as a critical region for CdC syndrome however, genotyp
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1857::0a8593e1934e2317efd210030cc9bd0f
https://dk.um.si/IzpisGradiva.php?id=66494
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9
MTHFR C677T and A1298C genotypes and haplotypes in Slovenian couples with unexplained infertility problems and in embryonic tissues from spontaneous abortions
Autor: Stangler Herodež, Špela, Zagradišnik, Boris, Erjavec Škerget, Alenka, Zagorac, Andreja, Takač, Iztok, Vlaisavljević, Veljko, Lokar, Lidija, Kokalj-Vokač, Nadja
Publikováno v: Balkan Journal of Medical Genetics, vol. 16, no. 1, pp. 31-39, 2013.
The objective of this study was to analyze the methylenetetrahydrofolate reductases (MTHFRs) C677T and A1298C genotype distributions in couples with unexplained fertility problems (UFP) and healthy controls, and to analyze the genotype and haplotype
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1857::f30785ca9a0cba86a849e7f860a0d207
https://dk.um.si/Dokument.php?id=110366&dn=
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