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Reassignment of HMX1 indicates copy number variation within 4p16.1 may be an alternative cause of oculoauricular phenotypes

Reassignment of HMX1 indicates copy number variation within 4p16.1 may be an alternative cause of oculoauricular phenotypes
Reassignment of HMX1 indicates copy number variation within 4p16.1 may be an alternative cause of oculoauricular phenotypes
copy number variation, 4p16.1, oculoauricular phenotypes, HMX1, evolutionarily conserved region, euchromatic variant.
1552-4825
Barber, John
4785a6e4-bd63-4230-ab61-41a0ae12c761
Barber, John
4785a6e4-bd63-4230-ab61-41a0ae12c761

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).

Record type: Letter
Text
Barber, 4p16.1 CNVs revised text 01-06-2018 HEFCE - Accepted Manuscript
Restricted to Repository staff only until 6 June 2019.
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More information

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: https://eprints.soton.ac.uk/id/eprint/421700
ISSN: 1552-4825
PURE UUID: 263bc8e6-c9a0-4b85-a33e-e984e8d3b223

Catalogue record

Date deposited: 21 Jun 2018 16:30
Last modified: 13 Mar 2019 18:24

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Author: John Barber

University divisions

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