Orvisky, E <br/><br/>
Glucosylsphingosine accumulation in mice and patients with type 2 Gaucher disease begins early in gestation.  [electronic resource] 

 -  Pediatric research  Aug 2000 
 - 233-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0031-3998 
<br/><br/><label>Standard No.: </label>10.1203/00006450-200008000-00018  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Chromatography, High Pressure Liquid<br/>Embryonic and Fetal Development<br/>Gaucher Disease--embryology<br/>Gestational Age<br/>Glucosylceramidase--genetics<br/>Heterozygote<br/>Humans<br/>Hydrops Fetalis--pathology<br/>Mice<br/>Mice, Mutant Strains<br/>Polymerase Chain Reaction<br/>Psychosine--analogs & derivatives<br/>Sphingosine--analogs & derivatives