Andonova S Online catalog

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Author Andonova S

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$Spinal muscular atrophy with congenital bone fractures 2 caused by a rare loss-of-function ASCC1 gene mutation in two Bulgarian Roma patients$

Article

Clinical genetics Spinal muscular atrophy with congenital bone fractures 2 caused by a rare loss-of-function ASCC1 gene mutation in two Bulgarian Roma patients

Bradinova I ; Andonova S ; Vazharova R ; Tomova S ; Balabanski L ; Savov A | Denmark | 26/03/2022

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Article

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society Pontocerebellar hypoplasia type 1 for the neuropediatrician: Genotype-phenotype correlations and diagnostic guidelines based on new cases and overview of the literature

Ivanov I, Author ; Atkinson D ; Litvinenko I ; Angelova L ; Andonova S ; Mumdjiev H ; Pacheva I ; Panova M ; Yordanova R ; Belovejdov V ; Petrova A ; Bosheva M ; Shmilev T ; Savov A ; Jordanova A | 03/04/2018

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