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A de novo microdeletion of 5p15.1 in a boy with autism spectrum disorder

A de novo microdeletion of 5p15.1 in a boy with autism spectrum disorder
A de novo microdeletion of 5p15.1 in a boy with autism spectrum disorder
0022-2593
pp.S95
Willatt, L.
ba28e5e6-92f8-4d46-bd82-8c9afd9b7012
Kenwrick, S.
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Parkin, G.
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Whittaker, J.
fbd09856-ad0d-44e4-9a33-3a904b70c0bc
Baralle, D.
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Willatt, L.
ba28e5e6-92f8-4d46-bd82-8c9afd9b7012
Kenwrick, S.
8b59e2f1-5666-4ce8-88a6-abe49347da9c
Parkin, G.
e4990535-7a03-4f03-bc1d-f821e8d65c5b
Whittaker, J.
fbd09856-ad0d-44e4-9a33-3a904b70c0bc
Baralle, D.
faac16e5-7928-4801-9811-8b3a9ea4bb91

Willatt, L., Kenwrick, S., Parkin, G., Whittaker, J. and Baralle, D. (2006) A de novo microdeletion of 5p15.1 in a boy with autism spectrum disorder. Journal of Medical Genetics, 43, pp.S95.

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Published date: 2006

Identifiers

Local EPrints ID: 60429
URI: http://eprints.soton.ac.uk/id/eprint/60429
ISSN: 0022-2593
PURE UUID: 4bbb16ed-57da-461f-afb7-d0c51d0b1173
ORCID for D. Baralle: ORCID iD orcid.org/0000-0003-3217-4833

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Date deposited: 13 Mar 2009
Last modified: 12 Dec 2021 03:40

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Contributors

Author: L. Willatt
Author: S. Kenwrick
Author: G. Parkin
Author: J. Whittaker
Author: D. Baralle ORCID iD

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