Stankiewicz, P <br/><br/>
[Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods].  [electronic resource] 

 -  Pediatria polska  Mar 1996 
 - 241-5 p.  digital 
<br/><br/> Publication Type: Case Reports; English Abstract; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0031-3939 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Chromosomes, Human, Pair 11<br/>Chromosomes, Human, Pair 22<br/>Craniofacial Abnormalities<br/>Cryptorchidism<br/>Cytogenetics--methods<br/>Genetic Markers<br/>Heart Failure<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant<br/>Intellectual Disability<br/>Male<br/>Translocation, Genetic--genetics<br/>Trisomy--diagnosis