Albaramki, J <br/><br/>
Sanjad Sakati syndrome: a case series from Jordan.  [electronic resource] 

 -  Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit  May 2012 
 - 527-31 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1020-3397 
<br/><br/><label>Standard No.: </label>10.26719/2012.18.5.527  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Child<br/>Child, Preschool<br/>Chromosomes, Human, Pair 1--genetics<br/>Consanguinity<br/>Female<br/>Genetic Testing<br/>Growth Disorders--diagnosis<br/>Humans<br/>Hypoparathyroidism--diagnosis<br/>Infant<br/>Infant, Newborn<br/>Intellectual Disability--diagnosis<br/>Jordan<br/>Male<br/>Molecular Chaperones--genetics<br/>Osteochondrodysplasias--diagnosis<br/>Phenotype<br/>Seizures--diagnosis