Faienza, M F <br/><br/>
P16INK4A gene homozygous deletions in human acute leukaemias with alterations of chromosome 9.  [electronic resource] 

 -  British journal of haematology  Jun 1996 
 - 632-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0007-1048 
<br/><br/><label>Standard No.: </label>10.1046/j.1365-2141.1996.d01-1674.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Burkitt Lymphoma--genetics<br/>Child<br/>Child, Preschool<br/>Chromosomes, Human, Pair 9<br/>Female<br/>Gene Deletion<br/>Homozygote<br/>Humans<br/>Leukemia, Myeloid, Acute--genetics<br/>Leukemia-Lymphoma, Adult T-Cell--genetics<br/>Male<br/>Molecular Sequence Data<br/>Polymerase Chain Reaction<br/>Precursor B-Cell Lymphoblastic Leukemia-Lymphoma--genetics<br/>Precursor Cell Lymphoblastic Leukemia-Lymphoma--genetics<br/>Purine-Nucleoside Phosphorylase--genetics