M. Kecmanović

发表

Polymorphisms of the Prion Protein Gene (PRNP) in a Serbian Population

V. Dobričić, S. Romac, R. Dimitrijević, 2010, The International journal of neuroscience.

Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats

V. Milic-Rasic, J. Dačković, S. Romac, 2016, Clinical chemistry and laboratory medicine.

Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot‐Marie‐Tooth patients

V. Milic-Rasic, J. Dačković, S. Romac, 2009, Journal of the peripheral nervous system : JPNS.

An algorithm for genetic testing of Serbian patients with demyelinating Charcot-Marie-Tooth.

V. Milic-Rasic, J. Dačković, S. Romac, 2013, Genetic testing and molecular biomarkers.

Coexistence of Unverricht‐Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidity

A. Ristić, D. Sokić, N. Vojvodić, 2009, Epilepsia.

Distribution of Y-chromosome haplogroups in Serbian population groups originating from historically and geographically significant distinct parts of the Balkan Peninsula.

M. Mihajlovic, D. Keckarević, M. Kecmanović, 2022, Forensic science international. Genetics.

Genetics of Lafora progressive myoclonic epilepsy: current perspectives

S. Romac, N. Jović, G. Stevanović, 2016, The application of clinical genetics.

GSTA1, GSTM1, GSTP1 and GSTT1 polymorphisms in progressive myoclonus epilepsy: A Serbian case–control study

T. Simić, D. Sokić, M. Matic, 2015, Seizure.

Schizophrenia and Apolipoprotein E Gene Polymorphism in Serbian Population

V. Dobričić, S. Romac, R. Dimitrijević, 2010, The International journal of neuroscience.

HD Phenocopies—Possible Role of Saitohin Gene

V. Dobričić, S. Romac, R. Dimitrijević, 2008, The International journal of neuroscience.

Identification of a broad spectrum of mammalian and avian species using the short fragment of the mitochondrially encoded cytochrome b gene

M. Andrejevic, Biljana N Bursać, D. Keckarević, 2019, Forensic Science, Medicine and Pathology.

MECP2 mutations in Serbian Rett syndrome patients

C. Klein, V. Dobričić, S. Romac, 2007, Acta neurologica Scandinavica.

A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression

S. Romac, D. Keckarević, M. Keckarević-Marković, 2012, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Assessment of mutation rates for PPY23 Y chromosome STR loci in Serbian father-son pairs.

D. Keckarević, M. Kecmanović, M. Keckarević Marković, 2019, Forensic science international. Genetics.

A comprehensive mutation study in wide deep-rooted R1b Serbian pedigree: mutation rates and male relative differentiation capacity of 36 Y-STR markers.

V. Čokić, Z. Jakovski, D. Keckarević, 2019, Forensic science international. Genetics.

Differentiation of Cannabis subspecies by THCA synthase gene analysis using RFLP.

D. Keckarević, M. Kecmanović, M. Keckarević Marković, 2017, Journal of Forensic and Legal Medicine.

Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin

S. Romac, N. Jović, G. Stevanović, 2016, Clinical genetics.

Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene

S. Romac, N. Jović, G. Stevanović, 2013, Journal of the Neurological Sciences.

A Shared Haplotype Indicates a Founder Event in Unverricht–Lundborg Disease Patients from Serbia

A. Ristić, D. Sokić, S. Romac, 2014, The International journal of neuroscience.