Parlier, V <br/><br/>
Trisomy 8 detection in granulomonocytic, erythrocytic and megakaryocytic lineages by chromosomal in situ suppression hybridization in a case of refractory anaemia with ringed sideroblasts complicating the course of paroxysmal nocturnal haemoglobinuria.  [electronic resource] 

 -  British journal of haematology  Jun 1992 
 - 296-304 p.  digital 
<br/><br/> Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0007-1048 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2141.1992.tb08223.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Anemia, Sideroblastic--etiology<br/>Chromosomes, Human, Pair 8<br/>DNA--analysis<br/>Erythrocytes--ultrastructure<br/>Granulocytes--ultrastructure<br/>Hemoglobinuria, Paroxysmal--complications<br/>Histocytological Preparation Techniques<br/>Humans<br/>Immunohistochemistry<br/>Karyotyping<br/>Male<br/>Megakaryocytes--ultrastructure<br/>Monocytes--ultrastructure<br/>Nucleic Acid Hybridization<br/>Trisomy