Ryan, S G <br/><br/>
Benign familial neonatal convulsions: evidence for clinical and genetic heterogeneity.  [electronic resource] 

 -  Annals of neurology  May 1991 
 - 469-73 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0364-5134 
<br/><br/><label>Standard No.: </label>10.1002/ana.410290504  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosomes, Human, Pair 20<br/>DNA--analysis<br/>Epilepsy--genetics<br/>Family<br/>Female<br/>Genetic Linkage<br/>Genetic Testing<br/>Genotype<br/>Humans<br/>Infant, Newborn<br/>Pedigree<br/>Phenotype<br/>Recombination, Genetic