Phelan, C M <br/><br/>
Chromosome 17 abnormalities and lack of TP53 mutations in paediatric central nervous system tumours.  [electronic resource] 

 -  Human genetics  Dec 1995 
 - 684-90 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/BF00210300  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Base Sequence<br/>Brain Neoplasms--genetics<br/>Child<br/>Child, Preschool<br/>Chromosome Aberrations<br/>Chromosome Deletion<br/>Chromosome Disorders<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 17<br/>Conserved Sequence<br/>DNA Primers<br/>Female<br/>Genes, p53<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Molecular Sequence Data<br/>Mutation<br/>Polymerase Chain Reaction<br/>Polymorphism, Restriction Fragment Length<br/>Spinal Cord Neoplasms--genetics<br/>Transcription, Genetic