Subrt, I <br/><br/>
A case of the 18p--syndrome.  [electronic resource] 

 -  Humangenetik  1972 
 - 359-60 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0018-7348 
<br/><br/><label>Standard No.: </label>10.1007/BF00283989  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--etiology<br/>Chromosome Aberrations--blood<br/>Chromosome Disorders<br/>Chromosomes, Human, 16-18<br/>Craniofacial Dysostosis--etiology<br/>Female<br/>Humans<br/>Immunoglobulin A--analysis<br/>Infant<br/>Karyotyping<br/>Skull--abnormalities