Publications
Export 2 results:
Filters: Keyword is Molecular Sequence Data and Author is Vissers, Lisenka E L M [Clear All Filters]
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. Am J Hum Genet. 2015 ;97(6):904-13.
. NR2F1 mutations cause optic atrophy with intellectual disability. Am J Hum Genet. 2014 ;94(2):303-9.
.