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Journal of Pediatric Genetics|August 22, 2022
Retrospective Diagnosis of Pontocerebellar Hypoplasia Type 1B in a Family with Two Deceased Newborn ChildrenIrena Bradinova, Silvia Andonova, Alexey SavovJournal of Pediatric Genetics|August 22, 2022
Triploidy in a Live-Born Extremely Low Birth Weight Twin: Clinical AspectsLiliya Vakrilova, Stanislava Hitrova-Nikolova, Irena BradinovaHealthcare (Basel, Switzerland)|April 26, 2025
Expectations and the Patient-Doctor Relationship: Ethical Considerations in a Case of TriploidyIliya Mangarov, Irena Bradinova, Ralitsa Georgieva, et al.American Journal of Medical Genetics. Part A|October 14, 2005
Hypertrichosis in patients with SURF1 mutationsElsebet Ostergaard, Irena Bradinova, Susanne Holst Ravn, et al.Clinical Case Reports|April 18, 2024
Netherton syndrome-A therapeutic challenge in childhoodPolina Kostova, Guergana Petrova, Martin Shahid, et al.Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|January 23, 2017
New Territory for an Old Disease: 5-Alpha-Reductase Type 2 Deficiency in BulgariaSilvia Andonova, Ralitsa Robeva, Radoslava Vazharova, et al.Journal of Medical Genetics|November 12, 2010
2q31.1 microdeletion syndrome: redefining the associated clinical phenotypeBoyan Dimitrov, Irina Balikova, Thomy de Ravel, et al.Journal of Genetics|February 1, 2023
Arginase deficiency in Bulgaria: first cases and potential endemic region for the disorderSlavena Atemin, Tihomir Todorov, Ivan Tourtourikov, et al.Pageof 1