Konrad, M <br/><br/>
Prenatal and postnatal management of hyperprostaglandin E syndrome after genetic diagnosis from amniocytes.  [electronic resource] 

 -  Pediatrics  Mar 1999 
 - 678-83 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1098-4275 
<br/><br/><label>Standard No.: </label>10.1542/peds.103.3.678  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amniotic Fluid--cytology<br/>Bartter Syndrome--diagnosis<br/>DNA Mutational Analysis<br/>Female<br/>Humans<br/>Indomethacin--therapeutic use<br/>Infant, Newborn<br/>Kidney--diagnostic imaging<br/>Male<br/>Polyhydramnios--drug therapy<br/>Polymorphism, Single-Stranded Conformational<br/>Potassium Channels<br/>Pregnancy<br/>Prenatal Diagnosis<br/>Prostaglandins E--blood<br/>Syndrome<br/>Ultrasonography