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Ludmila Bessonova

Showing results (1-10 of 4) with videos related to

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Genes|July 26, 2020
A Family Case of Congenital Myasthenic Syndrome-22 Induced by Different Combinations of Molecular Causes in SiblingsOlga Shchagina, Ludmila Bessonova, Igor Bychkov, et al.
Biomedicines|October 26, 2024
Common Variants in the <i>TYR</i> Gene with Unclear Pathogenicity as the Cause of Oculocutaneous Albinism in a Cohort of Russian PatientsOlga Shchagina, Anna Stepanova, Polina Mishakova, et al.
International Journal of Molecular Sciences|July 27, 2022
Complex Diagnostics of Non-Specific Intellectual Developmental DisorderOlga Levchenko, Elena Dadali, Ludmila Bessonova, et al.
Clinical Genetics|February 5, 2025
Rare Cause 5q SMA: Molecular Genetic and Clinical Analyses of Intragenic Subtle Variants in the SMN LocusKristina Mikhalchuk, Viktoria Zabnenkova, Svetlana Braslavskaya, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Genes|July 26, 2020
A Family Case of Congenital Myasthenic Syndrome-22 Induced by Different Combinations of Molecular Causes in SiblingsOlga Shchagina, Ludmila Bessonova, Igor Bychkov, et al.
Biomedicines|October 26, 2024
Common Variants in the <i>TYR</i> Gene with Unclear Pathogenicity as the Cause of Oculocutaneous Albinism in a Cohort of Russian PatientsOlga Shchagina, Anna Stepanova, Polina Mishakova, et al.
International Journal of Molecular Sciences|July 27, 2022
Complex Diagnostics of Non-Specific Intellectual Developmental DisorderOlga Levchenko, Elena Dadali, Ludmila Bessonova, et al.
Clinical Genetics|February 5, 2025
Rare Cause 5q SMA: Molecular Genetic and Clinical Analyses of Intragenic Subtle Variants in the SMN LocusKristina Mikhalchuk, Viktoria Zabnenkova, Svetlana Braslavskaya, et al.
Pageof 1