Выявление редкой наследственной патологии путем совершенствования медико-генетической помощи пациентам с врожденными пороками развития
Published in Медицинская генетика • Jan 1, 2015
NobleIDNI9P65W74R68S70
Authors:,
Л. И. Минайчева
Л. П. Назаренко
Abstract
The possibility of detection of rare hereditary diseases by improving the genetic health care for patients with congenital malformations is discussed. An algorithm of the follow-up of patients with congenital malformations is presented. The algorithm is a pattern of interaction of various health car...
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