Breuning, M H <br/><br/>
Partial trisomy 6p due to familial translocation t(6;20)(p21;p13). A new syndrome?  [electronic resource] 

 -  Human genetics  Aug 1977 
 - 7-13 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/BF00295802  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Birth Weight<br/>Child, Preschool<br/>Chromosomes, Human, 13-15<br/>Chromosomes, Human, 19-20<br/>Chromosomes, Human, 21-22 and Y<br/>Chromosomes, Human, 6-12 and X<br/>Female<br/>Genetic Linkage<br/>Heart Defects, Congenital--genetics<br/>Heterozygote<br/>Humans<br/>Kidney--abnormalities<br/>Pedigree<br/>Proteinuria--genetics<br/>Psychomotor Disorders--genetics<br/>Translocation, Genetic<br/>Trisomy