Abdalla, Ebtesam M <br/><br/>
Kyphoscoliotic type of Ehlers-Danlos Syndrome (EDS VIA) in six Egyptian patients presenting with a homogeneous clinical phenotype.  [electronic resource] 

 -  European journal of pediatrics  Jan 2015 
 - 105-12 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1432-1076 
<br/><br/><label>Standard No.: </label>10.1007/s00431-014-2429-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Child, Preschool<br/>Craniofacial Abnormalities--etiology<br/>Ehlers-Danlos Syndrome--diagnosis<br/>Female<br/>Humans<br/>Infant<br/>Male<br/>Phenotype<br/>Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase--deficiency