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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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