Courtens, W <br/><br/>
Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion.  [electronic resource] 

 -  Human genetics  Oct 1998 
 - 497-505 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/s004390050857  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Deletion<br/>Chromosome Inversion<br/>Chromosomes, Human, Pair 18<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant, Newborn<br/>Male<br/>Microsatellite Repeats<br/>Mothers<br/>Noonan Syndrome--genetics<br/>Phenotype<br/>Twins, Monozygotic--genetics