Barber, John (2018) Reassignment of HMX1 indicates copy number variation within 4p16.1 may be an alternative cause of oculoauricular phenotypes. American Journal of Medical Genetics part A. (doi:10.1002/ajmg.a.40385).
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Letter
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Barber, 4p16.1 CNVs revised text 01-06-2018 HEFCE
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Accepted/In Press date: 6 June 2018
e-pub ahead of print date: 28 July 2018
Keywords:
copy number variation, 4p16.1, oculoauricular phenotypes, HMX1, evolutionarily conserved region, euchromatic variant.
Identifiers
Local EPrints ID: 421700
URI: http://eprints.soton.ac.uk/id/eprint/421700
ISSN: 1552-4825
PURE UUID: 263bc8e6-c9a0-4b85-a33e-e984e8d3b223
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Date deposited: 21 Jun 2018 16:30
Last modified: 06 Jun 2024 04:04
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Author:
John Barber
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