Detection of Thrombophilic Mutations Related to Spontaneous Abortions by a Multiplex SNaPshot Method

Por Madjunkova, Svetlana, Volk, Marija, Peterlin, Borut, Plaseska-Karanfilska, Dijana
Publicado em 2012

Expression Signature as a Biomarker for Prenatal Diagnosis of Trisomy 21

Por Volk, Marija, Maver, Aleš, Lovrečić, Luca, Juvan, Peter, Peterlin, Borut
Publicado em 2013

Clinical utility of array comparative genomic hybridisation in prenatal setting

Por Lovrecic, Luca, Remec, Ziga Iztok, Volk, Marija, Rudolf, Gorazd, Writzl, Karin, Peterlin, Borut
Publicado no BMC Med Genet (2016)

Characterization of a de novo sSMC 17 detected in a girl with developmental delay and dysmorphic features

Por Stavber, Lana, Bertok, Sara, Kovač, Jernej, Volk, Marija, Lovrečić, Luca, Battelino, Tadej, Hovnik, Tinka
Publicado no Mol Cytogenet (2017)

Clinical and Molecular Cytogenetic Characterisation of Children with Developmental Delay and Dysmorphic Features

Por BERTOK, Sara, ŽERJAV TANŠEK, Mojca, KOTNIK, Primož, BATTELINO, Tadej, VOLK, Marija, PECILE, Vanna, CLEVA, Lisa, GASPARINI, Paolo, KOVAČ, Jernej, HOVNIK, Tinka
Publicado no Zdr Varst (2015)