Kennerknecht, I <br/><br/>
Dup(1q)(q42-->qter) syndrome: case report and review of literature.  [electronic resource] 

 -  American journal of medical genetics  Dec 1993 
 - 1157-60 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.1320470805  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Chromosomes, Human, Pair 1<br/>Developmental Disabilities--genetics<br/>Face--abnormalities<br/>Humans<br/>Infant<br/>Karyotyping<br/>Male<br/>Mouth Abnormalities--genetics<br/>Multigene Family<br/>Syndrome<br/>Trisomy