Nyholt, D R <br/><br/>
Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity.  [electronic resource] 

 -  Neurology  May 1998 
 - 1428-32 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0028-3878 
<br/><br/><label>Standard No.: </label>10.1212/wnl.50.5.1428  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Calcium Channels--genetics<br/>Chromosomes, Human, Pair 19<br/>Female<br/>Genetic Heterogeneity<br/>Genetic Linkage<br/>Humans<br/>Lod Score<br/>Male<br/>Microsatellite Repeats<br/>Migraine Disorders--genetics<br/>Pedigree<br/>Software<br/>Statistics, Nonparametric