Lyons, M J <br/><br/>
Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome.  [electronic resource] 

 -  Journal of medical genetics  Jan 2009 
 - 9-13 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.2008.060509  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Adolescent<br/>Amino Acid Substitution<br/>Child<br/>Child, Preschool<br/>Female<br/>Humans<br/>Male<br/>Mediator Complex<br/>X-Linked Intellectual Disability--diagnosis<br/>Muscle Hypotonia--diagnosis<br/>Mutation<br/>Phenotype<br/>Receptors, Thyroid Hormone--genetics<br/>Syndrome