Journal article

Atypical congenital dyserythropoietic anaemia: a novel mutation in LPIN2 causes Majeed syndrome with incomplete penetrance

Publication status:: Published

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APA Style

Roy, N., Babbs, C., Wilkinson, N., Godbold, E., Roberts, N., Ferguson, D., Sloane-Stanley, J., Robbe, P., McGowan, S., Hall, G., Qureshi, A., Atoyebi, W., Schuh, A., Roberts, D., & Higgs, D. (2013). Atypical congenital dyserythropoietic anaemia: a novel mutation in LPIN2 causes Majeed syndrome with incomplete penetrance. BRITISH JOURNAL OF HAEMATOLOGY, 161, 11–11.

MLA Style

Roy, N., et al. “Atypical Congenital Dyserythropoietic Anaemia: a Novel Mutation in LPIN2 Causes Majeed Syndrome with Incomplete Penetrance.” BRITISH JOURNAL OF HAEMATOLOGY, vol. 161, 2013, pp. 11–11.

Chicago Style

Roy, N, C Babbs, N Wilkinson, E Godbold, N Roberts, D Ferguson, J Sloane-Stanley, et al. 2013. “Atypical Congenital Dyserythropoietic Anaemia: a Novel Mutation in LPIN2 Causes Majeed Syndrome with Incomplete Penetrance.” BRITISH JOURNAL OF HAEMATOLOGY 161: 11–11.
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+ Roy, N More by this author

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+ Babbs, C More by this author

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+ Wilkinson, N More by this author

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+ Godbold, E More by this author

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+ Roberts, N More by this author

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Journal:: BRITISH JOURNAL OF HAEMATOLOGY More from this journal
Volume:: 161
Pages:: 11-11
Publication date:: 2013-04-01
ISSN:: 0007-1048

Pubs id:: pubs:399230
UUID:: uuid:b55d305d-3403-4327-abba-7f0b213811e3
Local pid:: pubs:399230
Source identifiers:: 399230
Deposit date:: 2013-11-16

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Copyright date:: 2013

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

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