Jones, Gabriela E <br/><br/>
Should we offer prenatal testing for 17q12 microdeletion syndrome to all cases with prenatally diagnosed echogenic kidneys? Prenatal findings in two families with 17q12 microdeletion syndrome and review of the literature.  [electronic resource] 

 -  Prenatal diagnosis  Dec 2015 
 - 1336-41 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Review 
<br/><br/><label>ISSN: </label>1097-0223 
<br/><br/><label>Standard No.: </label>10.1002/pd.4701  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnostic imaging<br/>Adult<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 17--diagnostic imaging<br/>Female<br/>Humans<br/>Infant<br/>Intellectual Disability--diagnostic imaging<br/>Kidney--diagnostic imaging<br/>Male<br/>Ultrasonography, Prenatal