Skip to content
Book Bag:
0
items
(Full)
Login
Language
English
Slovak
Catalog
Catalog Books
Articles
Catalog ONDV
Catalog OND
All Fields
Title
Author
Subject
Call Number
ISBN/ISSN
Find
Advanced
Active search for patients wit...
Cite this
Print
Export Record
Export to MARC
Export to BibTeX
Export to Jednoduchý textový výpis
Export to ISBD (text)
Export to Citácia ISO 690 (HTML)
Export to Citácia ISO 690 (.doc)
Add to Book Bag
Remove from Book Bag
Permanent link
Active search for patients with familial hypercholesterolemia in the Czech Republic
Bibliographic Details
Main Authors:
Freiberger, T.
(Author)
,
Grombiříková, Hana
(Author)
,
Kopálková, L.
(Author)
,
Kuhrová, V.
(Author)
,
Kozák, L.
(Author)
Corporate Author:
Nové trendy v prevencii aterosklerózy
(Author)
Format:
Conference Proceeding
Article
Language:
Slovak
English
Subjects:
hypercholesterolémia familiárna
projekt epidemiologického výskumu
apolipoproteín B
analýza DNA, mutačná
abstrakty z kongresu
dieťa
Česko
Pozri predplatné
Predplatné
Kliknite na „Pozri predplatné“.
Holdings
Description
Similar Items
Staff View
Similar Items
Discrepancies among genotype and phenotype in children and adolescents suffering from familial hypercholesterolemia
by: Kuhrová, V., et al.
Discrepancies among genotype and phenotype in children and adolescents suffering from familial hypercholesterolemia
by: Hyánek, Josef, 1933-, et al.
Familiárny defektný apo-B-100 u pacientov s fenotypom familiárnej hypercholesterolémie. Výsledky projektu MED PED v Slovenskej republike
by: Gašparovič, J., et al.
Súčasné možnosti DNA diagnostiky hyperfenylalaninémie (fenylketonúrie)
by: Ürge, Oto, et al.
Familiárny defektný APO-B-100 v rodinách s familiárnou hypercholesterolémiou a vo všeobecnej populácii
by: Gašparovič, J., et al.
Prev
Next
Similar Items
Discrepancies among genotype and phenotype in children and adolescents suffering from familial hypercholesterolemia
by: Kuhrová, V., et al.
Discrepancies among genotype and phenotype in children and adolescents suffering from familial hypercholesterolemia
by: Hyánek, Josef, 1933-, et al.
Familiárny defektný apo-B-100 u pacientov s fenotypom familiárnej hypercholesterolémie. Výsledky projektu MED PED v Slovenskej republike
by: Gašparovič, J., et al.
Súčasné možnosti DNA diagnostiky hyperfenylalaninémie (fenylketonúrie)
by: Ürge, Oto, et al.
Familiárny defektný APO-B-100 v rodinách s familiárnou hypercholesterolémiou a vo všeobecnej populácii
by: Gašparovič, J., et al.