The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy

by Gorazd Rudolf, Luca Lovrečić, Nataša Tul, Nataša Teran, Borut Peterlin
Published 2019-06-01

Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss.

by Tina Likar, Mensuda Hasanhodžić, Nataša Teran, Aleš Maver, Borut Peterlin, Karin Writzl
Published 2018-01-01

P182 ARTERIES IN PATIENTS WITH HUNTINGTON’S DISEASE

by Ziva Melik, Jan Kobal, Ksenija Cankar, Janja Pretnar, Marjan Zaletel, Lucijan Kobal, Natasa Teran
Published 2017-12-01

Clinical and Histopathological Features of Gelsolin Amyloidosis Associated with a Novel <i>GSN</i> Variant p.Glu580Lys

by Maja Potrč, Marija Volk, Matteo de Rosa, Jože Pižem, Nataša Teran, Helena Jaklič, Aleš Maver, Brigita Drnovšek-Olup, Michela Bollati, Katarina Vogelnik, Alojzija Hočevar, Ana Gornik, Vladimir Pfeifer, Borut Peterlin, Marko Hawlina, Ana Fakin
Published 2021-01-01