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PEDIA: prioritization of exome data by image analysis.
Genet Med. 2019 Dec;21(12):2807-2814. doi: 10.1038/s41436-019-0566-2. Epub 2019 Jun 5.
Genet Med. 2019.
PMID: 31164752
Free PMC article.
Brachytelephalangic chondrodysplasia punctata caused by new small hemizygous deletion in a boy presenting with hearing loss.
Vrečar I, Rudolf G, Peterlin B, Lovrecic L.
Vrečar I, et al.
Mol Cytogenet. 2015 Oct 31;8:83. doi: 10.1186/s13039-015-0187-7. eCollection 2015.
Mol Cytogenet. 2015.
PMID: 26526591
Free PMC article.
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Telegenetics: an Update on Availability and Use of Telemedicine in Clinical Genetics Service.
Vrečar I, Hristovski D, Peterlin B.
Vrečar I, et al.
J Med Syst. 2017 Feb;41(2):21. doi: 10.1007/s10916-016-0666-3. Epub 2016 Dec 17.
J Med Syst. 2017.
PMID: 27987158
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Further Clinical Delineation of the MEF2C Haploinsufficiency Syndrome: Report on New Cases and Literature Review of Severe Neurodevelopmental Disorders Presenting with Seizures, Absent Speech, and Involuntary Movements.
Vrečar I, Innes J, Jones EA, Kingston H, Reardon W, Kerr B, Clayton-Smith J, Douzgou S.
Vrečar I, et al.
J Pediatr Genet. 2017 Sep;6(3):129-141. doi: 10.1055/s-0037-1601335. Epub 2017 Apr 12.
J Pediatr Genet. 2017.
PMID: 28794905
Free PMC article.
Review.
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Direct-to-consumer genetic testing in Slovenia: availability, ethical dilemmas and legislation.
Vrecar I, Peterlin B, Teran N, Lovrecic L.
Vrecar I, et al.
Biochem Med (Zagreb). 2015;25(1):84-9. doi: 10.11613/BM.2015.010.
Biochem Med (Zagreb). 2015.
PMID: 25672471
Free PMC article.
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Content validity and inter-rater reliability of the Halliwick-concept-based instrument 'Swimming with Independent Measure'.
Sršen KG, Vidmar G, Pikl M, Vrečar I, Burja C, Krušec K.
Sršen KG, et al. Among authors: vrecar i.
Int J Rehabil Res. 2012 Jun;35(2):116-23. doi: 10.1097/MRR.0b013e32835277ab.
Int J Rehabil Res. 2012.
PMID: 22395426
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