Slade, Ingrid <br/><br/>
Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma.  [electronic resource] 

 -  Familial cancer  Jun 2011 
 - 337-42 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1573-7292 
<br/><br/><label>Standard No.: </label>10.1007/s10689-010-9411-0  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Cerebellar Neoplasms--genetics<br/>Child<br/>Child, Preschool<br/>Female<br/>Germ-Line Mutation<br/>Humans<br/>Male<br/>Medulloblastoma--genetics<br/>Middle Aged<br/>Patched Receptors<br/>Patched-1 Receptor<br/>Receptors, Cell Surface--genetics<br/>Repressor Proteins--genetics