Surace, C <br/><br/>
Mild ring 17 syndrome shares common phenotypic features irrespective of the chromosomal breakpoints location.  [electronic resource] 

 -  Clinical genetics  Sep 2009 
 - 256-62 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2009.01203.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Chromosome Breakage<br/>Chromosomes, Human, Pair 17--genetics<br/>Facies<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant<br/>Infant, Newborn<br/>Karyotyping<br/>Male<br/>Phenotype<br/>Physical Chromosome Mapping<br/>Ring Chromosomes<br/>Syndrome