Oliveira, Neide I S S <br/><br/>
Two different karyotypes with 1q abnormalities in a patient with Fanconi anemia.  [electronic resource] 

 -  Leukemia research  Nov 2002 
 - 1047-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0145-2126 
<br/><br/><label>Standard No.: </label>10.1016/s0145-2126(02)00038-3  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acute Disease<br/>Bone Marrow--pathology<br/>Child<br/>Chromosome Aberrations<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 1--genetics<br/>Fanconi Anemia--complications<br/>Humans<br/>Karyotyping<br/>Leukemia, Myeloid--complications<br/>Male