The role of genetic determinant in the development of severe perinatal asphyxia

The frequency of GSTT1 and GSTM1 gene deletion polymorphism was determined in a casecontrol study of fullterm Ukrainian newborns including patients with perinatal asphyxia. Multiplex polymerase chain reaction was used for genotyping 245 fullterm newborns.

Рубрика Биология и естествознание
Вид статья
Язык русский
Дата добавления 11.11.2012
Размер файла 88,6 K

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