Journal article

Hereditary haemochromatosis: pilot study of case-finding approach to early diagnosis in primary care.

Publication status:: Published

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APA Style

Emery, J., Rose, P., Harcourt, J., & Robson, K. (2001). Hereditary haemochromatosis: pilot study of case-finding approach to early diagnosis in primary care. AMERICAN JOURNAL OF HUMAN GENETICS, 69(4), 431–431.

MLA Style

Emery, J, et al. “Hereditary Haemochromatosis: Pilot Study of Case-Finding Approach to Early Diagnosis in Primary Care.” AMERICAN JOURNAL OF HUMAN GENETICS, vol. 69, no. 4, 2001, pp. 431–31.

Chicago Style

Emery, J, P Rose, J Harcourt, and K Robson. 2001. “Hereditary Haemochromatosis: Pilot Study of Case-Finding Approach to Early Diagnosis in Primary Care.” AMERICAN JOURNAL OF HUMAN GENETICS 69 (4): 431–31.
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Authors

+ Emery, J More by this author

Role:: Author

+ Rose, P More by this author

Role:: Author

+ Harcourt, J More by this author

Role:: Author

+ Robson, K More by this author

Institution:: University of Oxford
Division:: MSD
Department:: RDM
Sub department:: Weatherall Insti. of Molecular Medicine
Role:: Author

Journal:: AMERICAN JOURNAL OF HUMAN GENETICS More from this journal
Volume:: 69
Issue:: 4
Pages:: 431-431
Publication date:: 2001-10-01
ISSN:: 0002-9297

Pubs id:: pubs:214955
UUID:: uuid:e99fb217-3bb4-4ed6-a23b-0fcb3bc276fe
Local pid:: pubs:214955
Source identifiers:: 214955
Deposit date:: 2014-09-18
ARK identifier:: ark:/29072/ora_e99fb2173bb44ed6a23b0fcb3bc276fe

Terms of use

Copyright date:: 2001

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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