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Journal of Pediatric Genetics|April 24, 2023
Three Cases of Joubert Syndrome in a Consanguineous Syrian Family and a Interesting Case of Multinational CollaborationDavor Petrović, Vida Čulić, Zofia Swinderek-AlsayedMedical Science Monitor : International Medical Journal of Experimental and Clinical Research|October 1, 2011
Full trisomy 5 in a sample of spontaneous abortion and Arias Stella reactionVida Čulić, Bernarda Lozic, Ivana Kuzmić-Prusac, et al.Cytogenetic and Genome Research|November 23, 2018
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 LossVida Čulić, Ruzica Lasan-Trcić, Thomas Liehr, et al.Human Genome Variation|October 30, 2016
Distal arthrogryposis with variable clinical expression caused by <i>TNNI2</i> mutationVida Čulić, Noriko Miyake, Sunčana Janković, et al.Cytogenetic and Genome Research|April 13, 2021
Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental DelayStanislav A Vasilyev, Nikolay A Skryabin, Anna A Kashevarova, et al.Pageof 1