Klaphake, Sanne <br/><br/>
A patient with chromosome 18p deletion and congenital hypoglossia.  [electronic resource] 

 -  Clinical dysmorphology  Apr 2018 
 - 46-48 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1473-5717 
<br/><br/><label>Standard No.: </label>10.1097/MCD.0000000000000207  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosome Disorders--genetics<br/>Chromosomes, Human, Pair 18--genetics<br/>Female<br/>Holoprosencephaly--genetics<br/>Humans<br/>Infant, Newborn<br/>Karyotyping<br/>Stomatognathic System Abnormalities--genetics