Showing 1 - 20 results of 31 for search 'E. L. Dadali', query time: 0.69s
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Lamb–Shaffer syndrome, deferred outside not described by SOX5 mutation by I. V. Sharkova, E. L. Dadali
Published 2018-04-01
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Diagnostic criteria for spinal muscular atrophy 5q by I. V. Sharkova, E. L. Dadali, S. S. Nikitin
Published 2021-12-01
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Aymé–Gripp syndrome in a Russian patient with a newly detected mutation in the MAF gene by E. L. Dadali, T. V. Markova, O. P. Ryzhkova
Published 2021-12-01
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Genetic heterogeneity of hereditary diseases of nervous system: problems and solutions by E. L. Dadali, E. K. Ginter, A. B. Polyakov
Published 2015-02-01
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Proximal spinal muscular atrophy types I-IV: Specific features of molecular genetic diagnosis by V. V. Zabnenkova, E. L. Dadali, A. V. Polyakov
Published 2015-02-01
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Stiff-person syndrome with early onset in infancy by S. A. Malmberg, E. L. Dadali, D. B. Jumakchanov, A. Kch. Djaksibaeva
Published 2015-06-01
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Clinical and genetic characteristics and diagnosis of hereditary variants of neonatal epilepsy by N. A. Semenova, E. L. Dadali, A. A. Sharkov, I. A. Akimova
Published 2017-11-01
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Gillespiе syndrome, caused by previously undescribed mutation in the gene <i>ITPR1<i> by I. V. Sharkova, I. A. Akimova, O. V. Khlebnikova, E. L. Dadali
Published 2019-05-01
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GENETICS OF MENTAL RETARDATION by A. V. Lavrov, A. V. Bannikov, A. I. Chausheva, E. L. Dadali
Published 2017-01-01
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Comparative analysis of features phenotype limb-girdle muscular dystrophy 2А and 2I types by I. V. Sharkova, E. L. Dadali, O. P. Ryzhkova, V. N. Evdokimenkov
Published 2015-02-01
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POLR3A-related hypomyelinating leukodystrophy: case report and literature review by A. F. Murtazina, T. V. Markova, A. A. Orlova, O. P. Ryzhkova, O. A. Shchagina, E. L. Dadali
Published 2021-12-01
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