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Elena O. Belyaeva

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Delineation of Clinical Manifestations of the Inherited Xq24 Microdeletion Segregating with sXCI in Mothers: Two Novel Cases with Distinct Phenotypes Ranging from UBE2A Deficiency Syndrome to Recurrent Pregnancy Loss.

2020 Cytogenetic and Genome Research
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Анализ спектра мутаций в генах COL1A1 и COL1A2 с использованием массового параллельного секвенирования у больных несовершенным остеогенезом в Томской области: Analysis of mutation spectrum of COL1A1 and COL1A2 genes using massively parallel sequencing in patients with osteogenesis imperfecta in the Tomsk region

2020
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