Steinberg, S J <br/><br/>
Peroxisomal disorders: clinical and biochemical studies in 15 children and prenatal diagnosis in 7 families.  [electronic resource] 

 -  American journal of medical genetics  Aug 1999 
 - 502-10 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cells, Cultured<br/>Child<br/>Child, Preschool<br/>Female<br/>Fibroblasts--pathology<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Peroxisomal Disorders--diagnosis<br/>Phenotype<br/>Phytanic Acid--blood<br/>Pregnancy<br/>Prenatal Diagnosis<br/>Ultrasonography, Prenatal<br/>Zellweger Syndrome--diagnosis