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Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.
Dazzo E, Fanciulli M, Serioli E, Minervini G, Pulitano P, Binelli S, Di Bonaventura C, Luisi C, Pasini E, Striano S, Striano P, Coppola G, Chiavegato A, Radovic S, Spadotto A, Uzzau S, La Neve A, Giallonardo AT, Mecarelli O, Tosatto SC, Ottman R, Michelucci R, Nobile C. Dazzo E, et al. Among authors: radovic s. Am J Hum Genet. 2015 Jun 4;96(6):992-1000. doi: 10.1016/j.ajhg.2015.04.020. Am J Hum Genet. 2015. PMID: 26046367 Free PMC article.
Exome Capture with Heterologous Enrichment in Pig (Sus scrofa).
Guiatti D, Pomari E, Radovic S, Spadotto A, Stefanon B. Guiatti D, et al. Among authors: radovic s. PLoS One. 2015 Oct 2;10(10):e0139328. doi: 10.1371/journal.pone.0139328. eCollection 2015. PLoS One. 2015. PMID: 26431395 Free PMC article.
De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise.
Writzl K, Maver A, Kovačič L, Martinez-Valero P, Contreras L, Satrustegui J, Castori M, Faivre L, Lapunzina P, van Kuilenburg ABP, Radović S, Thauvin-Robinet C, Peterlin B, Del Arco A, Hennekam RC. Writzl K, et al. Among authors: radovic s. Am J Hum Genet. 2017 Nov 2;101(5):844-855. doi: 10.1016/j.ajhg.2017.09.017. Am J Hum Genet. 2017. PMID: 29100094 Free PMC article.
A physical, genetic and functional sequence assembly of the barley genome.
International Barley Genome Sequencing Consortium; Mayer KF, Waugh R, Brown JW, Schulman A, Langridge P, Platzer M, Fincher GB, Muehlbauer GJ, Sato K, Close TJ, Wise RP, Stein N. International Barley Genome Sequencing Consortium, et al. Nature. 2012 Nov 29;491(7426):711-6. doi: 10.1038/nature11543. Epub 2012 Oct 17. Nature. 2012. PMID: 23075845 Free article.
124 results