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Luca Lovrecic

Showing results (1-10 of 22) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|August 19, 2007
Sodium phenylbutyrate in Huntington's disease: a dose-finding studyPenelope Hogarth, Luca Lovrecic, Dimitri Krainc
BMC Cancer|June 4, 2021
Identification of women at risk for hereditary breast and ovarian cancer in a sample of 1000 Slovenian women: a comparison of guidelinesUrska Kotnik, Borut Peterlin, Luca Lovrecic
Molecular Syndromology|July 8, 2016
A New Case of an Extremely Rare 3p21.31 Interstitial DeletionLuca Lovrecic, Sara Bertok, Mojca Žerjav Tanšek
Prenatal Diagnosis|April 19, 2023
The genetic approach to stillbirth: A »systematic review«Maja Dolanc Merc, Borut Peterlin, Luca Lovrecic
Scientific Reports|March 31, 2023
Assessment of pathogenic variation in gynecologic cancer genes in a national cohortUrška Kotnik, Aleš Maver, Borut Peterlin, et al.
Biochemia Medica|February 13, 2015
Direct-to-consumer genetic testing in Slovenia: availability, ethical dilemmas and legislationIrena Vrecar, Borut Peterlin, Natasa Teran, et al.
Molecular Cytogenetics|November 4, 2015
Brachytelephalangic chondrodysplasia punctata caused by new small hemizygous deletion in a boy presenting with hearing lossIrena Vrečar, Gorazd Rudolf, Borut Peterlin, et al.
Prenatal Diagnosis|May 30, 2024
Further exploration of cardiac channelopathy and cardiomyopathy genes in stillbirthMaja Dolanc Merc, Urška Kotnik, Borut Peterlin, et al.
Current Opinion in Clinical Nutrition and Metabolic Care|May 24, 2015
Nutriepigenomics: the role of nutrition in epigenetic control of human diseasesMarlene Remely, Barbara Stefanska, Luca Lovrecic, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2017
Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 casesGaber Bergant, Ales Maver, Luca Lovrecic, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Movement Disorders : Official Journal of the Movement Disorder Society|August 19, 2007
Sodium phenylbutyrate in Huntington's disease: a dose-finding studyPenelope Hogarth, Luca Lovrecic, Dimitri Krainc
BMC Cancer|June 4, 2021
Identification of women at risk for hereditary breast and ovarian cancer in a sample of 1000 Slovenian women: a comparison of guidelinesUrska Kotnik, Borut Peterlin, Luca Lovrecic
Molecular Syndromology|July 8, 2016
A New Case of an Extremely Rare 3p21.31 Interstitial DeletionLuca Lovrecic, Sara Bertok, Mojca Žerjav Tanšek
Prenatal Diagnosis|April 19, 2023
The genetic approach to stillbirth: A »systematic review«Maja Dolanc Merc, Borut Peterlin, Luca Lovrecic
Scientific Reports|March 31, 2023
Assessment of pathogenic variation in gynecologic cancer genes in a national cohortUrška Kotnik, Aleš Maver, Borut Peterlin, et al.
Biochemia Medica|February 13, 2015
Direct-to-consumer genetic testing in Slovenia: availability, ethical dilemmas and legislationIrena Vrecar, Borut Peterlin, Natasa Teran, et al.
Molecular Cytogenetics|November 4, 2015
Brachytelephalangic chondrodysplasia punctata caused by new small hemizygous deletion in a boy presenting with hearing lossIrena Vrečar, Gorazd Rudolf, Borut Peterlin, et al.
Prenatal Diagnosis|May 30, 2024
Further exploration of cardiac channelopathy and cardiomyopathy genes in stillbirthMaja Dolanc Merc, Urška Kotnik, Borut Peterlin, et al.
Current Opinion in Clinical Nutrition and Metabolic Care|May 24, 2015
Nutriepigenomics: the role of nutrition in epigenetic control of human diseasesMarlene Remely, Barbara Stefanska, Luca Lovrecic, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2017
Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 casesGaber Bergant, Ales Maver, Luca Lovrecic, et al.
Pageof 3