Struthers, J L <br/><br/>
Parental origin of the isochromosome 12p in Pallister-Killian syndrome: molecular analysis of one patient and review of the reported cases.  [electronic resource] 

 -  American journal of medical genetics  May 1999 
 - 111-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Review 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Child<br/>Chromosomes, Human, Pair 12<br/>Fathers<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Intellectual Disability--genetics<br/>Isochromosomes<br/>Male<br/>Microsatellite Repeats<br/>Models, Genetic<br/>Mothers<br/>Pedigree<br/>Phenotype<br/>Skin Pigmentation--genetics<br/>Syndrome