Facet browsing currently unavailable
Page 1 of 1 results
Sort by: relevance publication year
Showing DOI matching
10.17352/jnnsd.000017
Absence of CHRDL1 and FOXC1 sequence changes in two brothers with Megalocornea-Mental Retardation Syndrome JOURNAL ARTICLE published 3 July 2017 in Journal of Neurology, Neurological Science and Disorders |