Schluth-Bolard, Caroline <br/><br/>
TWIST microdeletion identified by array CGH in a patient presenting Saethre-Chotzen phenotype and a complex rearrangement involving chromosomes 2 and 7.  [electronic resource] 

 -  European journal of medical genetics   
 - 156-64 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1769-7212 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2007.12.003  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acrocephalosyndactylia--genetics<br/>Adult<br/>Child, Preschool<br/>Chromosomes, Human, Pair 2--genetics<br/>Chromosomes, Human, Pair 7--genetics<br/>Female<br/>Gene Deletion<br/>Gene Rearrangement<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Nuclear Proteins--genetics<br/>Nucleic Acid Hybridization<br/>Oligonucleotide Array Sequence Analysis<br/>Phenotype<br/>Twist-Related Protein 1--genetics