Thompson, L J <br/><br/>
Unique and recurrent WAS gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia.  [electronic resource] 

 -  Blood cells, molecules & diseases   
 - 218-26 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article 
<br/><br/><label>ISSN: </label>1079-9796 
<br/><br/><label>Standard No.: </label>10.1006/bcmd.1999.0247  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Asian People--genetics<br/>Black People--genetics<br/>Family Health<br/>Female<br/>Genetic Carrier Screening<br/>Haplotypes<br/>Humans<br/>Male<br/>Mutation--genetics<br/>Pedigree<br/>Polymorphism, Single-Stranded Conformational<br/>Pregnancy<br/>Prenatal Diagnosis<br/>Sequence Analysis, DNA<br/>Thrombocytopenia--genetics<br/>United Kingdom--epidemiology<br/>White People--genetics<br/>Wiskott-Aldrich Syndrome--genetics<br/>X Chromosome