Mencarelli, Maria Antonietta <br/><br/>
Clinical and molecular characterization of a patient with a 2q31.2-32.3 deletion identified by array-CGH.  [electronic resource] 

 -  American journal of medical genetics. Part A  Apr 2007 
 - 858-65 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.31602  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 2<br/>Craniofacial Abnormalities<br/>Family Health<br/>Humans<br/>Infant, Newborn<br/>Intellectual Disability<br/>Male<br/>Mental Disorders<br/>Nucleic Acid Hybridization<br/>Oligonucleotide Array Sequence Analysis<br/>Sleep Wake Disorders