Aitken, D A <br/><br/>
Prenatal detection of a probable heterozygote for ADA deficiency and severe combined immunodeficiency disease using a microradioassay.  [electronic resource] 

 -  Clinical genetics  Apr 1980 
 - 293-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.1980.tb00150.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Deaminase--blood<br/>Amniotic Fluid--cytology<br/>Cells, Cultured<br/>Consanguinity<br/>Erythrocytes--enzymology<br/>Female<br/>Fetal Blood--enzymology<br/>Fibroblasts--enzymology<br/>Heterozygote<br/>Humans<br/>Immunologic Deficiency Syndromes--enzymology<br/>Infant, Newborn<br/>Microchemistry<br/>Nucleoside Deaminases--deficiency<br/>Phenotype<br/>Pregnancy<br/>Prenatal Diagnosis<br/>Protein Deficiency--diagnosis