Pierquin, G <br/><br/>
Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndrome.  [electronic resource] 

 -  Human genetics  Sep 1991 
 - 587-91 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/BF00209018  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Chromosome Banding<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 1<br/>Chromosomes, Human, Pair 6<br/>Collagen--metabolism<br/>Face--abnormalities<br/>Female<br/>Humans<br/>Infant<br/>Joint Dislocations--diagnosis<br/>Karyotyping<br/>Male<br/>Pedigree<br/>Phenotype<br/>Skin--metabolism<br/>Syndrome<br/>Trisomy