Fuleihan, R <br/><br/>
Localization of the genetic defect in X-linked immunoglobulin deficiency with normal or elevated IgM (HIGMX-1) to the CD40 ligand gene.  [electronic resource] 

 -  Transactions of the Association of American Physicians  1993 
 - 91-5 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>0066-9458 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Antigens, CD--metabolism<br/>Antigens, Differentiation, B-Lymphocyte--metabolism<br/>CD40 Antigens<br/>CD40 Ligand<br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Dysgammaglobulinemia--complications<br/>Gene Expression<br/>Genetic Linkage<br/>Humans<br/>Hypergammaglobulinemia--complications<br/>IgA Deficiency--complications<br/>IgG Deficiency--complications<br/>Immunoglobulin M--blood<br/>In Vitro Techniques<br/>Male<br/>Membrane Glycoproteins--genetics<br/>Pedigree<br/>RNA, Messenger--genetics<br/>T-Lymphocytes--immunology<br/>X Chromosome