Bartsch, O <br/><br/>
A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region.  [electronic resource] 

 -  Human genetics  Oct 1997 
 - 669-75 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/s004390050571  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Child<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 18--genetics<br/>Chromosomes, Human, Pair 21--genetics<br/>Down Syndrome--genetics<br/>Female<br/>Humans<br/>Infant<br/>Intellectual Disability--genetics<br/>Male<br/>Pedigree<br/>Telomere<br/>Translocation, Genetic--genetics