Guioli, S <br/><br/>
Kallmann syndrome due to a translocation resulting in an X/Y fusion gene.  [electronic resource] 

 -  Nature genetics  Aug 1992 
 - 337-40 p.  digital 
<br/><br/> Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1061-4036 
<br/><br/><label>Standard No.: </label>10.1038/ng0892-337  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Base Sequence<br/>Cloning, Molecular<br/>Exons<br/>Humans<br/>Introns<br/>Kallmann Syndrome--genetics<br/>Male<br/>Molecular Sequence Data<br/>Oligodeoxyribonucleotides<br/>Polymerase Chain Reaction--methods<br/>Recombination, Genetic<br/>Restriction Mapping<br/>Sequence Homology, Amino Acid<br/>Sequence Homology, Nucleic Acid<br/>Translocation, Genetic<br/>X Chromosome<br/>Y Chromosome