Ishida, Hiroyuki <br/><br/>
GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia.  [electronic resource] 

 -  European journal of pediatrics  Aug 2012 
 - 1273-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1432-1076 
<br/><br/><label>Standard No.: </label>10.1007/s00431-012-1715-7  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Female<br/>GATA2 Transcription Factor--genetics<br/>Genetic Markers<br/>Humans<br/>Immunologic Deficiency Syndromes--diagnosis<br/>Lymphedema--diagnosis<br/>Mutation, Missense<br/>Myelodysplastic Syndromes--diagnosis<br/>Phenotype<br/>Syndrome<br/>Young Adult