al-Ghamdi, M A <br/><br/>
Arthrogryposis multiplex congenita, craniofacial, and ophthalmological abnormalities and normal intelligence: a new syndrome?  [electronic resource] 

 -  American journal of medical genetics  Sep 1997 
 - 401-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/(sici)1096-8628(19970905)71:4<401::aid-ajmg6>3.0.co;2-w  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--classification<br/>Child<br/>Craniofacial Abnormalities--classification<br/>Diagnosis, Differential<br/>Eye Abnormalities--classification<br/>Female<br/>Humans<br/>Intelligence<br/>Male<br/>Radiography<br/>Syndrome