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The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1

The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1
The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1
3805573073
62-68
Karger
Macdonald, D.
de17722c-713a-44d7-b445-6fe5bc0b206a
Reiter, A.
8fc082eb-6b46-4412-86b2-f4c7669f0650
Cross, N.C.P.
f87650da-b908-4a34-b31b-d62c5f186fe4
Bain, B.J.
Macdonald, D.
de17722c-713a-44d7-b445-6fe5bc0b206a
Reiter, A.
8fc082eb-6b46-4412-86b2-f4c7669f0650
Cross, N.C.P.
f87650da-b908-4a34-b31b-d62c5f186fe4
Bain, B.J.

Macdonald, D., Reiter, A. and Cross, N.C.P. (2003) The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1. In, Bain, B.J. (ed.) Chronic Myeloproliferative Disorders: Cytogenetic and Molecular Genetic Abnormalities. Basel, Switzerland. Karger, pp. 62-68. (doi:10.1159/000068098).

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Published date: 2003

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Local EPrints ID: 60004
URI: http://eprints.soton.ac.uk/id/eprint/60004
ISBN: 3805573073
PURE UUID: e4cfb642-8265-4a6a-8f56-a9d381475a88
ORCID for N.C.P. Cross: ORCID iD orcid.org/0000-0001-5481-2555

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Date deposited: 28 Oct 2008
Last modified: 16 Mar 2024 03:23

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Contributors

Author: D. Macdonald
Author: A. Reiter
Author: N.C.P. Cross ORCID iD
Editor: B.J. Bain

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