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
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Vasilishina A.A.,
Bulatnikova M.A.,
Kotelevskaya E.A.,
Smolyaninov A.B.,
Larionova V.I.
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в сборнике European Journal of Human Genetics (European Human Genetics Conference, Abstracts), издательство Nature Publishing Group (United Kingdom), том 21, тезисы, с. 475-475
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