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HD phenocopies--possible role of Saitohin gene.
Janković N, Kecmanović M, Dimitrijević R, Keckarević Marković M, Dobricić V, Keckarević D, Savić Pavicević D, Romac S. Janković N, et al. Among authors: dobricic v. Int J Neurosci. 2008 Mar;118(3):391-7. doi: 10.1080/00207450701593103. Int J Neurosci. 2008. PMID: 18300012
Human Y-specific STR haplotypes in population of Serbia and Montenegro.
Stevanović M, Dobricić V, Keckarević D, Perović A, Savić-Pavićević D, Keckarević-Marković M, Jovanović A, Romac S. Stevanović M, et al. Among authors: dobricic v. Forensic Sci Int. 2007 Sep 13;171(2-3):216-21. doi: 10.1016/j.forsciint.2006.05.038. Epub 2006 Jun 30. Forensic Sci Int. 2007. PMID: 16806776
MECP2 mutations in Serbian Rett syndrome patients.
Djarmati A, Dobricić V, Kecmanović M, Marsh P, Jancić-Stefanović J, Klein C, Djurić M, Romac S. Djarmati A, et al. Among authors: dobricic v. Acta Neurol Scand. 2007 Dec;116(6):413-9. doi: 10.1111/j.1600-0404.2007.00893.x. Acta Neurol Scand. 2007. PMID: 17986102
Polymorphisms of the prion protein gene (PRNP) in a Serbian population.
Dimitrijević R, Cadez I, Keckarević-Marković M, Keckarević D, Kecmanović M, Dobricić V, Savić-Pavićević D, Brajusković G, Romac S. Dimitrijević R, et al. Among authors: dobricic v. Int J Neurosci. 2010 Jul;120(7):496-501. doi: 10.3109/00207451003765907. Int J Neurosci. 2010. PMID: 20583902
Schizophrenia and apolipoprotein E gene polymorphism in Serbian population.
Kecmanović M, Dobricić V, Dimitrijević R, Keckarević D, Savić-Pavićević D, Keckarević-Marković M, Ivkovic M, Romac S. Kecmanović M, et al. Among authors: dobricic v. Int J Neurosci. 2010 Jul;120(7):502-6. doi: 10.3109/00207451003765956. Int J Neurosci. 2010. PMID: 20583903
Multidimensional aspects of pain in myotonic dystrophies.
Peric M, Peric S, Rapajic N, Dobricic V, Savic-Pavicevic D, Nesic I, Radojicic S, Novakovic I, Lavrnic D, Rakocevic-Stojanovic V. Peric M, et al. Among authors: dobricic v. Acta Myol. 2015 Dec;34(2-3):126-32. Acta Myol. 2015. PMID: 27199540 Free PMC article.
Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans.
Lohmann K, Masuho I, Patil DN, Baumann H, Hebert E, Steinrücke S, Trujillano D, Skamangas NK, Dobricic V, Hüning I, Gillessen-Kaesbach G, Westenberger A, Savic-Pavicevic D, Münchau A, Oprea G, Klein C, Rolfs A, Martemyanov KA. Lohmann K, et al. Among authors: dobricic v. Hum Mol Genet. 2017 Mar 15;26(6):1078-1086. doi: 10.1093/hmg/ddx018. Hum Mol Genet. 2017. PMID: 28087732 Free PMC article.
146 results