Reis, E <br/><br/>
Using a standard form to collect psychosocial data about hemophilia patients.  [electronic resource] 

 -  Health & social work  Aug 1982 
 - 206-14 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S. 
<br/><br/><label>ISSN: </label>0360-7283 
<br/><br/><label>Standard No.: </label>10.1093/hsw/7.3.206  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Data Collection<br/>Family<br/>Forms and Records Control--methods<br/>Hemophilia A--psychology<br/>Humans<br/>Male<br/>Medical Records<br/>Social Work<br/>Socioeconomic Factors<br/>Wisconsin