Agolini, E <br/><br/>
Expanding the clinical and molecular spectrum of PRMT7 mutations: 3 additional patients and review.  [electronic resource] 

 -  Clinical genetics  03 2018 
 - 675-681 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/cge.13137  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Alleles<br/>Comparative Genomic Hybridization<br/>Consanguinity<br/>Female<br/>Genetic Association Studies--methods<br/>Genetic Predisposition to Disease<br/>Genotype<br/>Humans<br/>Karyotype<br/>Male<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Protein-Arginine N-Methyltransferases--genetics<br/>Radiography<br/>Young Adult