%0 Journal Article
%U http://www.molvis.org/molvis/v19/311
%> mv-v19-311.pdf
%A  Vergult,  Sarah
%A  Leroy,  Bart
%A  Claerhout,  Ilse
%A  Menten,  Björn
%T Familial cases of a submicroscopic Xp22.2 deletion: genotype-phenotype correlation in microphthalmia with linear skin defects syndrome
%D 2013
%V 19
%P 311-318
%J Molecular Vision