Pinard, J M <br/><br/>
Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene.  [electronic resource] 

 -  Journal of neurology, neurosurgery, and psychiatry  Aug 1994 
 - 914-20 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0022-3050 
<br/><br/><label>Standard No.: </label>10.1136/jnnp.57.8.914  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Cerebral Cortex--abnormalities<br/>Child<br/>Congenital Abnormalities--diagnosis<br/>Epilepsy--etiology<br/>Female<br/>Genes, Dominant--genetics<br/>Genetic Counseling<br/>Genetic Linkage--genetics<br/>Humans<br/>Infant<br/>Intellectual Disability--etiology<br/>Magnetic Resonance Imaging<br/>Male<br/>Pedigree<br/>Sex Chromosome Aberrations--diagnosis<br/>X Chromosome