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Showing results (11-20 of 15) with videos related to

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Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|June 29, 2021
[Autosomal dominant spastic paraplegias]G E Rudenskaya, V A Kadnikova, L A Bessonova, et al.
International Journal of Molecular Sciences|December 9, 2023
Complex Chromosomal Rearrangement Involving Chromosomes 10 and 11, Accompanied by Two Adjacent 11p14.1p13 and 11p13p12 Deletions, Identified in a Patient with WAGR SyndromeAndrey V Marakhonov, Tatyana A Vasilyeva, Marina E Minzhenkova, et al.
International Journal of Molecular Sciences|October 26, 2024
Masks of Albinism: Clinical Spectrum of Hermansky-Pudlak SyndromeAnastasia M Bobreshova, Sofya A Ionova, Vitaly V Kadyshev, et al.
Human Mutation|March 26, 2019
Noncompaction cardiomyopathy is caused by a novel in-frame desmin (DES) deletion mutation within the 1A coiled-coil rod segment leading to a severe filament assembly defectAndrey V Marakhonov, Andreas Brodehl, Roman P Myasnikov, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|October 6, 2025
[Modern approaches to the diagnosis and treatment of Dravet syndrome in the Russian Federation. (Literature review and resolution of the Expert Council)]V I Guzeva, S I Kutsev, A S Petrukhin, et al.
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Showing results (11-20 of 15) with videos related to

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Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|June 29, 2021
[Autosomal dominant spastic paraplegias]G E Rudenskaya, V A Kadnikova, L A Bessonova, et al.
International Journal of Molecular Sciences|December 9, 2023
Complex Chromosomal Rearrangement Involving Chromosomes 10 and 11, Accompanied by Two Adjacent 11p14.1p13 and 11p13p12 Deletions, Identified in a Patient with WAGR SyndromeAndrey V Marakhonov, Tatyana A Vasilyeva, Marina E Minzhenkova, et al.
International Journal of Molecular Sciences|October 26, 2024
Masks of Albinism: Clinical Spectrum of Hermansky-Pudlak SyndromeAnastasia M Bobreshova, Sofya A Ionova, Vitaly V Kadyshev, et al.
Human Mutation|March 26, 2019
Noncompaction cardiomyopathy is caused by a novel in-frame desmin (DES) deletion mutation within the 1A coiled-coil rod segment leading to a severe filament assembly defectAndrey V Marakhonov, Andreas Brodehl, Roman P Myasnikov, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|October 6, 2025
[Modern approaches to the diagnosis and treatment of Dravet syndrome in the Russian Federation. (Literature review and resolution of the Expert Council)]V I Guzeva, S I Kutsev, A S Petrukhin, et al.
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