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 |
| Предмет | Cytology and genetics |
| Вид | статья |
| Язык | русский |
| Прислал(а) | Gorovenko |
| Дата добавления | 11.11.2012 |
| Размер файла | 88,6 K |
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