EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)
Publication year
2016Source
European Journal of Human Genetics, 24, 4, (2016), pp. 479-495ISSN
Publication type
Article / Letter to editor

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Organization
Laboratory Medicine
Journal title
European Journal of Human Genetics
Volume
vol. 24
Issue
iss. 4
Page start
p. 479
Page end
p. 495
Subject
Radboudumc 11: Renal disorders RIMLS: Radboud Institute for Molecular Life SciencesThis item appears in the following Collection(s)
- Academic publications [232014]
- Electronic publications [115251]
- Faculty of Medical Sciences [89012]
- Open Access publications [82626]
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