Slayton, William B <br/><br/>
Lineage-specific trisomy 21 in a neonate with resolving transient myeloproliferative syndrome.  [electronic resource] 

 -  Journal of pediatric hematology/oncology   
 - 224-6 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>1077-4114 
<br/><br/><label>Standard No.: </label>10.1097/00043426-200203000-00013  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Antigens, CD--metabolism<br/>Cell Lineage--genetics<br/>Chromosomes, Human, Pair 21--genetics<br/>Down Syndrome--genetics<br/>Erythrocytes<br/>Female<br/>Hematopoietic Stem Cells<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant, Newborn<br/>Karyotyping<br/>Monocytes<br/>Mosaicism--genetics<br/>Myeloproliferative Disorders--genetics