Jehee, Fernanda Sarquis <br/><br/>
An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome.  [electronic resource] 

 -  American journal of medical genetics. Part A  Dec 2005 
 - 221-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.30991  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Chromosomes, Human, X--genetics<br/>Face--abnormalities<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Intellectual Disability--genetics<br/>Male<br/>Microsatellite Repeats--genetics<br/>Microtubule-Associated Proteins--genetics<br/>Nucleic Acid Hybridization--genetics<br/>Pedigree<br/>Sex Chromosome Aberrations<br/>Sex Chromosome Disorders--genetics<br/>Transcription Factors--genetics