Autor:	Norio, Reijo
Předmět:	GENETIC disorders FAMILIAL diseases MOLECULAR genetics ALPHA fetoproteins ELECTROCARDIOGRAPHY HEART disease diagnosis MAGNETIC resonance imaging
Zdroj:	Human Genetics; May2003, Vol. 112 Issue 5/6, p470-526, 57p
Abstrakt:	This article is the third and last in a series entitled The Finnish Disease Heritage I–III. All the 36 rare hereditary diseases belonging to this entity are described for clinical and molecular genetic purposes, based on the Finnish experience gathered over a period of half a century. In addition, five other diseases are mentioned. They may be included in the list of the "Finnish diseases" after adequate complementary studies. [ABSTRACT FROM AUTHOR]
Databáze:	Complementary Index
Externí odkaz:	Zobrazit plný text záznamu Full text from SpringerLink