Tabori, U <br/><br/>
Detection of RAG mutations and prenatal diagnosis in families presenting with either T-B- severe combined immunodeficiency or Omenn's syndrome.  [electronic resource] 

 -  Clinical genetics  Apr 2004 
 - 322-6 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2004.00227.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Consanguinity<br/>DNA Mutational Analysis<br/>DNA-Binding Proteins--genetics<br/>Family Health<br/>Female<br/>Homeodomain Proteins--genetics<br/>Homozygote<br/>Humans<br/>Male<br/>Mutation, Missense<br/>Nuclear Proteins<br/>Polymorphism, Genetic<br/>Pregnancy<br/>Prenatal Diagnosis--methods<br/>Religion<br/>Severe Combined Immunodeficiency--diagnosis