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Borut Peterlin

Showing results (161-170 of 274) with videos related to

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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.
Croatian Medical Journal|March 3, 2020
DNMT3B rs1569686 and rs2424913 gene polymorphisms are associated with positive family history of preterm birth and smoking statusAnita Barišić, Maja Kolak, Ana Peterlin, 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.
Cells|January 8, 2023
Expression of Markers of Endometrial Receptivity in Obese Infertile PCOS Women before and after the Weight Loss Program-A Preliminary StudyGaber Bergant, Dzhamilyat Abdulkhalikova, Ana Šuštaršič, et al.
Pageof 28

Showing results (161-170 of 274) with videos related to

Sort By:
Pageof 28
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.
Croatian Medical Journal|March 3, 2020
DNMT3B rs1569686 and rs2424913 gene polymorphisms are associated with positive family history of preterm birth and smoking statusAnita Barišić, Maja Kolak, Ana Peterlin, 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.
Cells|January 8, 2023
Expression of Markers of Endometrial Receptivity in Obese Infertile PCOS Women before and after the Weight Loss Program-A Preliminary StudyGaber Bergant, Dzhamilyat Abdulkhalikova, Ana Šuštaršič, et al.
Pageof 28