Williams, C A <br/><br/>
Angelman syndrome in a daughter with del(15) (q11q13) associated with brachycephaly, hearing loss, enlarged foramen magnum, and ataxia in the mother.  [electronic resource] 

 -  American journal of medical genetics  Mar 1989 
 - 333-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.1320320312  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Ataxia--genetics<br/>Blotting, Southern<br/>Child, Preschool<br/>Chromosome Banding<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 15<br/>DNA--genetics<br/>Female<br/>Foramen Magnum--pathology<br/>Head--abnormalities<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Karyotyping<br/>Pedigree<br/>Speech Disorders--genetics<br/>Syndrome