Absence of CHRDL1 and FOXC1 sequence changes in two brothers with Megalocornea-Mental Retardation Syndrome
Crossref DOI link: https://doi.org/10.17352/jnnsd.000017
Published Online: 2017-07-03
Update policy: https://doi.org/10.17352/crossmark-policy
Gebril, OH
Cheong, SS
Hardcastle, AJ
Abdelraouf, ER
Eid, SR
Version of Record valid from 2013-11-25
Accepted Manuscript valid from 2015-05-25