Swinkels, Mariëlle E M <br/><br/>
Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype.  [electronic resource] 

 -  American journal of medical genetics. Part A  Jun 2008 
 - 1430-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.32310  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 9--genetics<br/>Craniofacial Abnormalities--genetics<br/>Cytokines--genetics<br/>DNA Mutational Analysis<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant, Newborn<br/>Intellectual Disability--genetics<br/>Male<br/>Muscle Hypotonia--genetics<br/>Netherlands<br/>Phenotype<br/>Syndrome