- Abstract:
-
OBJECTIVES: To test the feasibility of adopting and evaluating a systematic case-finding approach to the early diagnosis of hereditary haemochromatosis (HHC) in primary care, and to estimate the prevalence of presenting conditions for which HHC testing could be offered. METHODS: Systematic identification of, and genotyping for, C282Y and H63D mutations in patients presenting in primary care with possible symptoms of HHC during a 4-week period to 1 of 14 doctors in Oxfordshire. RESULTS: From ...
Expand abstract - Publisher copy:
- 10.1159/000066689
-
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- Journal:
- Community genetics
- Volume:
- 5
- Issue:
- 4
- Pages:
- 262-265
- Publication date:
- 2002
- DOI:
- EISSN:
-
1422-2833
- ISSN:
-
1422-2795
- URN:
-
uuid:8454d8ac-7831-4bae-ba5b-e8c500428ddc
- Source identifiers:
-
214428
- Local pid:
- pubs:214428
- Language:
- English
- Keywords:
- Copyright date:
- 2002
Journal article
Pilot study of early diagnosis of hereditary haemochromatosis through systematic case finding in primary care.
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