deMello, D E <br/><br/>
Molecular and phenotypic variability in the congenital alveolar proteinosis syndrome associated with inherited surfactant protein B deficiency.  [electronic resource] 

 -  The Journal of pediatrics  Jul 1994 
 - 43-50 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0022-3476 
<br/><br/><label>Standard No.: </label>10.1016/s0022-3476(94)70119-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Female<br/>Frameshift Mutation<br/>Gene Expression<br/>Genotype<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Lung--chemistry<br/>Male<br/>Phenotype<br/>Proteolipids--adverse effects<br/>Pulmonary Alveolar Proteinosis--congenital<br/>Pulmonary Surfactant-Associated Proteins<br/>Pulmonary Surfactants--adverse effects