European Journal of Human Genetics (European Human Genetics Conference, Abstracts)сборник

Статьи, опубликованные в сборнике

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• • 2013 A case of early diagnosis of 1p36 deletion in a girl with multiple congenital abnormalities including pulmonary lobulation defect, tetralogy Fallot, and early onset of focal epilepsy
  • Vasilishina A.A., Bulatnikova M.A., Kotelevskaya E.A., Smolyaninov A.B., Larionova V.I.
  • в сборнике European Journal of Human Genetics (European Human Genetics Conference, Abstracts), издательство Nature Publishing Group (United Kingdom), том 21, тезисы, с. 475-475
• • 2013 A case of hypomyelination - oligodontia - extrapyramidal signs -ataxia syndrome (Pol3 - associated hypomyelinating disorder)
  • Bulatnikova M.A., Vasilishina A.A., Smolyaninov A.B., Larionova V.I.
  • в сборнике European Journal of Human Genetics (European Human Genetics Conference, Abstracts), издательство Nature Publishing Group (United Kingdom), том 21, тезисы, с. 104-104