Petković, I <br/><br/>
Unusual segregation of t(11;22) resulting from crossing-over followed by 3:1 disjunction at meiosis I.  [electronic resource] 

 -  Clinical genetics  Dec 1996 
 - 515-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.1996.tb02725.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Anaphase<br/>Aneuploidy<br/>Chromosome Aberrations--genetics<br/>Chromosome Disorders<br/>Chromosomes, Human, Pair 11--genetics<br/>Chromosomes, Human, Pair 22--genetics<br/>Crossing Over, Genetic<br/>Face--abnormalities<br/>Female<br/>Humans<br/>Infant<br/>Intellectual Disability--genetics<br/>Karyotyping<br/>Male<br/>Muscle Hypotonia--genetics<br/>Nondisjunction, Genetic<br/>Phenotype<br/>Spermatogenesis<br/>Translocation, Genetic