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NCBIDiseaseCorpus
Documents
(787)
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# proj.
# Ann.
updated_at
PubMed
10077651
Mechanism of increased iron absorption in murine model of hereditary hemochromatosis: increased duod
1.81 KB
2015-11-04
10
6
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PubMed
10078732
Neurophysiologic follow-up of long-term dietary treatment in adult-onset adrenoleukodystrophy. OBJEC
1.69 KB
2015-11-20
9
9
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PubMed
10078749
GCH1 mutation in a patient with adult-onset oromandibular dystonia. The authors report a mutation in
417 Bytes
2015-11-02
18
5
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PubMed
10083733
Germline mutations of the APC gene in Korean familial adenomatous polyposis patients. We extensively
1.4 KB
2015-11-02
10
11
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PubMed
10083734
Molecular epidemiology of C9 deficiency heterozygotes with an Arg95Stop mutation of the C9 gene in J
1.27 KB
2015-11-02
11
6
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PubMed
10085150
The hereditary hemochromatosis protein, HFE, specifically regulates transferrin-mediated iron uptake
2.1 KB
2015-11-02
32
4
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PubMed
10090880
Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships an
1.64 KB
2015-11-06
12
9
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PubMed
10090885
Autoimmune lymphoproliferative syndrome with defective Fas: genotype influences penetrance. Autoimmu
1.73 KB
2015-11-02
11
10
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PubMed
10090890
Multicentric origin of hemochromatosis gene (HFE) mutations. Genetic hemochromatosis (GH) is believe
1.51 KB
2015-11-06
11
8
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PubMed
10094552
A retrospective anonymous pilot study in screening newborns for HFE mutations in Scandinavian popula
787 Bytes
2015-11-02
11
1
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