Petit, P <br/><br/>
A chromosomal abnormality (21q-) in primary thrombocytosis.  [electronic resource] 

 -  Human genetics  1979 
 - 105-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/BF00295597  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Chromosome Deletion<br/>Chromosomes, Human, 21-22 and Y<br/>Female<br/>Humans<br/>Thrombocytosis--genetics