Hereditary haemochromatosis: pilot study of case-finding approach to early diagnosis in primary care. - ORA - Oxford University Research Archive

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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. (2016). 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, 2016, pp. 431–31.

Chicago Style

Emery, J, P Rose, J Harcourt, and K Robson. 2016. “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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+ Emery, J More by this author

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+ Rose, P More by this author

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+ Harcourt, J More by this author

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+ Robson, K More by this author

Institution:

University of Oxford

Division:

MSD

Department:

RDM

Sub department:

Weatherall Insti. of Molecular Medicine

Role:

Author

Bibliographic Details

Journal:: AMERICAN JOURNAL OF HUMAN GENETICS
Volume:: 69
Issue:: 4
Pages:: 431-431
Publication date:: 2001-10-01
ISSN:: 0002-9297
Source identifiers:: 214955

Item Description

Pubs id:: pubs:214955
UUID:: uuid:e99fb217-3bb4-4ed6-a23b-0fcb3bc276fe
Local pid:: pubs:214955
Deposit date:: 2014-09-18

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Copyright date:: 2001

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

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