Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia
Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia
437-441
Ott, C. E.
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Hein, H.
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Lohan, S.
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Hoogeboom, J.
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Foulds, N.
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Grunhagen, J.
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Stricker, S.
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Villavicencio-Lorini, P.
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Klopocki, E.
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Mundlos, S.
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July 2012
Ott, C. E.
265dd736-c5b2-4b8d-a456-86d4b9728914
Hein, H.
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Lohan, S.
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Hoogeboom, J.
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Foulds, N.
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Grunhagen, J.
08ef903b-fdea-40ff-b2a6-db45efbb57bd
Stricker, S.
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Villavicencio-Lorini, P.
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Klopocki, E.
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Mundlos, S.
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Ott, C. E., Hein, H., Lohan, S., Hoogeboom, J., Foulds, N., Grunhagen, J., Stricker, S., Villavicencio-Lorini, P., Klopocki, E. and Mundlos, S.
(2012)
Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia.
Journal of Medical Genetics, 49 (7), .
(doi:10.1136/jmedgenet-2012-100825).
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Accepted/In Press date: 20 June 2012
Published date: July 2012
Organisations:
Human Development & Health
Identifiers
Local EPrints ID: 340590
URI: http://eprints.soton.ac.uk/id/eprint/340590
ISSN: 0022-2593
PURE UUID: 94258746-6d3f-4606-a131-7a66b5ea3e64
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Date deposited: 26 Jun 2012 10:52
Last modified: 14 Mar 2024 11:26
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Contributors
Author:
C. E. Ott
Author:
H. Hein
Author:
S. Lohan
Author:
J. Hoogeboom
Author:
N. Foulds
Author:
J. Grunhagen
Author:
S. Stricker
Author:
P. Villavicencio-Lorini
Author:
E. Klopocki
Author:
S. Mundlos
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