Whitelaw, A G <br/><br/>
Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosis.  [electronic resource] 

 -  Journal of medical genetics  Jun 1979 
 - 189-96 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0022-2593 
<br/><br/><label>Standard No.: </label>10.1136/jmg.16.3.189  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Alleles<br/>Anemia, Hemolytic, Congenital Nonspherocytic--diagnosis<br/>Edema--genetics<br/>Female<br/>Fetal Diseases--genetics<br/>Genetic Carrier Screening<br/>Genetic Variation<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Pregnancy<br/>Prenatal Diagnosis