about
Longevity and carrying the C282Y mutation for haemochromatosis on the HFE gene: case control study of 492 French centenariansFour variants in transferrin and HFE genes as potential markers of iron deficiency anaemia risk: an association study in menstruating women.Heterozygosity for the haemochromatosis mutation HFE C282Y is not a risk factor for angina.Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients.Targeted screening for genetic haemochromatosis: a combined phenotype/genotype approachRust and corrosion in hematopoietic stem cell transplantation: the problem of iron and oxidative stress.Heteroduplex analysis for the three common HFE variants: methodology, reliability and analysis of over 5000 requests for testing.Iron overload in myelodysplastic syndromes (MDS) - diagnosis, management, and response criteria: a proposal of the Austrian MDS platform
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
HFE Mutations as risk factors in disease.
@ast
HFE Mutations as risk factors in disease.
@en
HFE Mutations as risk factors in disease.
@nl
type
label
HFE Mutations as risk factors in disease.
@ast
HFE Mutations as risk factors in disease.
@en
HFE Mutations as risk factors in disease.
@nl
prefLabel
HFE Mutations as risk factors in disease.
@ast
HFE Mutations as risk factors in disease.
@en
HFE Mutations as risk factors in disease.
@nl
P356
P1476
HFE Mutations as risk factors in disease.
@en
P2093
Mark Worwood
P304
P356
10.1053/BEHA.2002.0005
P577
2002-06-01T00:00:00Z