Milica P. Markovic-Keckarevic

Belgrade, SE, Serbia

Last Updated: 09/26/2026

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Found 13 publications

Genetic Variability of Roma Population in Serbia: The Perspective From Uniparentally Inherited Markers.

Genetic Variability of Roma Population in Serbia: The Perspective From Uniparentally Inherited Markers.

Journal: American journal of human biology : the official journal of the Human Biology Council
Published: November 28, 2024

Genetic variability of Roma population in Serbia: The perspective from autosomal STR markers.

Genetic variability of Roma population in Serbia: The perspective from autosomal STR markers.

Journal: Journal of anthropological sciences = Rivista di antropologia : JASS
Published: July 14, 2024

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

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

Journal: Forensic science international. Genetics
Published: December 31, 2018

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

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

Journal: Forensic science international. Genetics
Published: September 13, 2018

Comparison of different methods of DNA recovery and PCR amplification in STR profiling of casings-a retrospective study.

Comparison of different methods of DNA recovery and PCR amplification in STR profiling of casings-a retrospective study.

Journal: International journal of legal medicine
Published: December 05, 2017

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

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

Journal: Journal of forensic and legal medicine
Published: January 23, 2017

Genetics of Lafora progressive myoclonic epilepsy: current perspectives.

Genetics of Lafora progressive myoclonic epilepsy: current perspectives.

Journal: The application of clinical genetics
Published: May 20, 2016

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

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

Journal: Clinical genetics
Published: June 25, 2014

A shared haplotype indicates a founder event in Unverricht-Lundborg disease patients from Serbia.

A shared haplotype indicates a founder event in Unverricht-Lundborg disease patients from Serbia.

Journal: The International journal of neuroscience
Published: July 26, 2013

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

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

Journal: Genetic testing and molecular biomarkers
Published: November 21, 2012

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

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

Journal: Journal of the neurological sciences
Published: September 27, 2012

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

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

Journal: Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
Published: January 05, 2012
Showing 1-12 of 13

Last Updated: 09/26/2026