Scott, H <br/><br/>
Familial opsonization defect associated with fatal infantile dermatitis, infections, and histiocytosis.  [electronic resource] 

 -  Archives of disease in childhood  Apr 1975 
 - 311-7 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1468-2044 
<br/><br/><label>Standard No.: </label>10.1136/adc.50.4.311  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Anti-Bacterial Agents--therapeutic use<br/>Bacterial Infections--complications<br/>Blood Transfusion<br/>Bronchopneumonia--complications<br/>Complement System Proteins--analysis<br/>Dermatitis--complications<br/>Female<br/>Histiocytes<br/>Histiocytosis, Langerhans-Cell--complications<br/>Humans<br/>Immunologic Deficiency Syndromes--complications<br/>Infant<br/>Infant, Newborn<br/>Lymph Nodes--pathology<br/>Male<br/>Opsonin Proteins<br/>Osteomyelitis--complications<br/>Phagocytosis<br/>Saccharomyces cerevisiae<br/>Sepsis--complications<br/>Skin--pathology<br/>Staphylococcus--isolation & purification<br/>Thymus Gland--pathology