Taschner, P E <br/><br/>
Chromosome 16 microdeletion in a patient with juvenile neuronal ceroid lipofuscinosis (Batten disease).  [electronic resource] 

 -  American journal of human genetics  Mar 1995 
 - 663-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Base Sequence<br/>Child<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 16<br/>Haplotypes<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Neuronal Ceroid-Lipofuscinoses--genetics<br/>Pedigree<br/>Polymerase Chain Reaction<br/>Sequence Deletion