Maier, R F <br/><br/>
HFE gene mutation and transferrin saturation in very low birthweight infants.  [electronic resource] 

 -  Archives of disease in childhood. Fetal and neonatal edition  Sep 1999 
 - F144-5 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1359-2998 
<br/><br/><label>Standard No.: </label>10.1136/fn.81.2.f144  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Female<br/>Genotype<br/>HLA Antigens--genetics<br/>Hemochromatosis Protein<br/>Histocompatibility Antigens Class I--genetics<br/>Humans<br/>Infant, Newborn<br/>Infant, Very Low Birth Weight--blood<br/>Male<br/>Membrane Proteins<br/>Mutation<br/>Prospective Studies<br/>Retrospective Studies<br/>Transferrin--metabolism