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Molecular Cytogenetics|June 29, 2018
Microduplication in the 2p16.1p15 chromosomal region linked to developmental delay and intellectual disabilityLuca Lovrecic, Chiara Gnan, Federica Baldan, et al.
Frontiers in Medicine|September 26, 2019
Vaginal Microbiome Signature Is Associated With Spontaneous Preterm DeliveryKeli Hočevar, Aleš Maver, Marijana Vidmar Šimic, et al.
Croatian Medical Journal|January 5, 2017
Genetic variation in leptin and leptin receptor genes is a risk factor for idiopathic recurrent spontaneous abortionAndrijana Müller, Jasenka Wagner, Alenka Hodžić, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Cornelia de Lange syndrome caused by heterozygous deletions of chromosome 8q24: comments on the article by Pereza et al. [2012]Nina Pereza, Srećko Severinski, Saša Ostojić, et al.
Frontiers in Neuroscience|November 29, 2023
Applicability of clinical genetic testing for deep brain stimulation treatment in monogenic Parkinson's disease and monogenic dystonia: a multidisciplinary team perspectiveValentino Rački, Mario Hero, Eliša Papić, et al.
Frontiers in Medicine|August 23, 2023
Oral microbiome and preterm birthMarijana Vidmar Šimic, Aleš Maver, Ana Nyasha Zimani, et al.
American Journal of Medical Genetics. Part A|February 9, 2012
Third case of 8q23.3-q24.13 deletion in a patient with Langer-Giedion syndrome phenotype without TRPS1 gene deletionNina Pereza, Srećko Severinski, Saša Ostojić, et al.
Frontiers in Genetics|January 27, 2022
Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic LanguagesNina Pereza, Rifet Terzić, Dijana Plaseska-Karanfilska, et al.
Clinical Genetics|October 1, 2024
Second Case of Gonadal Mosaicism and a Novel Nonsense NR2F1 Gene Variant as the Cause of Bosch-Boonstra-Schaaf Optic Atrophy SyndromeNenad Hrvatin, Nina Pereza, Tea Čaljkušić-Mance, et al.
Neurology. Genetics|March 4, 2022
Axonal Polyneuropathy in 2 Brothers With a Homozygous Missense Variant in the First Catalytic Domain of <i>PCYT2</i>Lea Leonardis, Marusa Skrjanec Pusenjak, Ales Maver, et al.
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