A recombinant chromosome 15 with duplication of the Prader-Willi/Angelman syndrome critical region arising from a familial intrachromosomal insertion, previously described as a paracentric inversion of 15q11-q15
A recombinant chromosome 15 with duplication of the Prader-Willi/Angelman syndrome critical region arising from a familial intrachromosomal insertion, previously described as a paracentric inversion of 15q11-q15
pp.S24
Collinson, M.
3941a8b6-83e6-4350-a8ef-a3331ec5ba44
Roberts, S.E.
1ba6b93b-6904-4bf4-b83d-600372bf6c60
Crolla, J.A.
c5f23751-8de9-4a55-9cc5-ca2fb635769c
Dennis, N.R.
154aa617-52e2-4711-98ef-89fef8610de7
2002
Collinson, M.
3941a8b6-83e6-4350-a8ef-a3331ec5ba44
Roberts, S.E.
1ba6b93b-6904-4bf4-b83d-600372bf6c60
Crolla, J.A.
c5f23751-8de9-4a55-9cc5-ca2fb635769c
Dennis, N.R.
154aa617-52e2-4711-98ef-89fef8610de7
Collinson, M., Roberts, S.E., Crolla, J.A. and Dennis, N.R.
(2002)
A recombinant chromosome 15 with duplication of the Prader-Willi/Angelman syndrome critical region arising from a familial intrachromosomal insertion, previously described as a paracentric inversion of 15q11-q15.
Journal of Medical Genetics, 39, .
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Published date: 2002
Identifiers
Local EPrints ID: 60527
URI: http://eprints.soton.ac.uk/id/eprint/60527
ISSN: 0022-2593
PURE UUID: 52347c59-09f4-4b5f-96b8-b665e92f7254
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Date deposited: 16 Mar 2009
Last modified: 11 Dec 2021 18:02
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Contributors
Author:
M. Collinson
Author:
S.E. Roberts
Author:
J.A. Crolla
Author:
N.R. Dennis
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