Whibley, Annabel C <br/><br/>
Fine-scale survey of X chromosome copy number variants and indels underlying intellectual disability.  [electronic resource] 

 -  American journal of human genetics  Aug 2010 
 - 173-88 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2010.06.017  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Breakage<br/>Chromosome Segregation--genetics<br/>Chromosomes, Human, X--genetics<br/>Cohort Studies<br/>DNA Copy Number Variations--genetics<br/>Disease--genetics<br/>Female<br/>Gene Rearrangement--genetics<br/>Genes, X-Linked--genetics<br/>Humans<br/>INDEL Mutation--genetics<br/>Intellectual Disability--genetics<br/>Male<br/>Oligonucleotide Array Sequence Analysis<br/>Pedigree<br/>Reproducibility of Results<br/>Retroelements--genetics<br/>Sequence Deletion--genetics