Verstraeten, L <br/><br/>
Biochemical diagnosis of a fatal case of Günther's disease in a newborn with hydrops foetalis.  [electronic resource] 

 -  European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies  Mar 1993 
 - 121-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0939-4974 
<br/><br/><label>Standard No.: </label>10.1515/cclm.1993.31.3.121  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aminolevulinic Acid--urine<br/>Erythrocytes--chemistry<br/>Feces--chemistry<br/>Humans<br/>Hydrops Fetalis--complications<br/>Infant, Newborn<br/>Infant, Premature, Diseases--diagnosis<br/>Lymphocytes--chemistry<br/>Male<br/>Mutation<br/>Porphyria, Erythropoietic--complications<br/>Porphyrins--analysis