Papagrigorakis, Manolis J <br/><br/>
De novo inv(2)(p12q34) associated with Klippel-Feil anomaly and hypodontia.  [electronic resource] 

 -  European journal of pediatrics  Sep 2003 
 - 594-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0340-6199 
<br/><br/><label>Standard No.: </label>10.1007/s00431-003-1262-3  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Adolescent<br/>Anodontia--diagnosis<br/>Chromosome Inversion<br/>Chromosomes, Human, Pair 2--genetics<br/>Congenital Hypothyroidism<br/>Facial Asymmetry--congenital<br/>Female<br/>Hearing Loss--congenital<br/>Humans<br/>Hypothyroidism--diagnosis<br/>Klippel-Feil Syndrome--diagnosis<br/>Psychomotor Disorders--congenital<br/>Radiography<br/>Scoliosis--congenital<br/>Speech Disorders--diagnosis<br/>Spine--diagnostic imaging