Zackai, E H <br/><br/>
Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction.  [electronic resource] 

 -  American journal of medical genetics  1980 
 - 507-21 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.1320070412  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Chromosomes, Human, 21-22 and Y<br/>Chromosomes, Human, 6-12 and X<br/>Female<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Intellectual Disability--genetics<br/>Karyotyping<br/>Male<br/>Meiosis<br/>Pedigree<br/>Phenotype<br/>Translocation, Genetic<br/>Trisomy