Gijsbers, A C J <br/><br/>
A subtle familial translocation t(3;21)(p26.3;q22.3): an apparently healthy boy with a 3p deletion and 21q duplication.  [electronic resource] 

 -  Cytogenetic and genome research  Jun 2010 
 - 245-9 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1424-859X 
<br/><br/><label>Standard No.: </label>10.1159/000302497  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Child, Preschool<br/>Chromosomes, Human, Pair 21<br/>Chromosomes, Human, Pair 3<br/>Face--abnormalities<br/>Family<br/>Female<br/>Humans<br/>Intellectual Disability--genetics<br/>Karyotyping<br/>Male<br/>Oligonucleotide Array Sequence Analysis<br/>Segmental Duplications, Genomic<br/>Sequence Deletion<br/>Translocation, Genetic<br/>Trisomy