Fryns, J P <br/><br/>
Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1).  [electronic resource] 

 -  American journal of medical genetics  Dec 1990 
 - 546-7 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.1320370425  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adolescent<br/>Chromosomes, Human, Pair 5<br/>Chromosomes, Human, Pair 7<br/>Female<br/>Genes, Recessive<br/>Humans<br/>Incisor--abnormalities<br/>Intellectual Disability--genetics<br/>Muscle Hypotonia--genetics<br/>Mutation<br/>Obesity--genetics<br/>Syndrome<br/>Translocation, Genetic