Brunner, H G <br/><br/>
Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathy.  [electronic resource] 

 -  Neurology  Jan 1991 
 - 80-4 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.41.1.80  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Chromosomes, Human, Pair 17<br/>Chromosomes, Human, Pair 19<br/>DNA--analysis<br/>Electromyography<br/>Female<br/>Genetic Linkage<br/>Hereditary Sensory and Motor Neuropathy--complications<br/>Humans<br/>Male<br/>Middle Aged<br/>Myotonic Dystrophy--complications<br/>Pedigree<br/>Physical Examination