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Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay.
Vasilyev SA, Skryabin NA, Kashevarova AA, Tolmacheva EN, Savchenko RR, Vasilyeva OY, Lopatkina ME, Zarubin AA, Fishman VS, Belyaeva EO, Filippova MO, Shorina AR, Maslennikov AB, Shestovskikh OL, Gayner TA, Čulić V, Vulić R, Nazarenko LP, Lebedev IN. Vasilyev SA, et al. Among authors: culic v. Cytogenet Genome Res. 2021;161(3-4):105-119. doi: 10.1159/000514491. Epub 2021 Apr 13. Cytogenet Genome Res. 2021. PMID: 33849037 Free article.
A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss.
Čulić V, Lasan-Trcić R, Liehr T, Lebedev IN, Pivić M, Pavelic J, Vulić R. Čulić V, et al. Cytogenet Genome Res. 2018;156(4):179-184. doi: 10.1159/000494822. Epub 2018 Nov 23. Cytogenet Genome Res. 2018. PMID: 30466092
Down syndrome: parental origin, recombination, and maternal age.
Vraneković J, Božović IB, Grubić Z, Wagner J, Pavlinić D, Dahoun S, Bena F, Culić V, Brajenović-Milić B. Vraneković J, et al. Among authors: culic v. Genet Test Mol Biomarkers. 2012 Jan;16(1):70-3. doi: 10.1089/gtmb.2011.0066. Epub 2011 Aug 23. Genet Test Mol Biomarkers. 2012. PMID: 21861707 Free PMC article.
135 results