Kariminejad, Ariana <br/><br/>
Intellectual disability, muscle weakness and characteristic face in three siblings: A newly described recessive syndrome mapping to 3p24.3-p25.3.  [electronic resource] 

 -  American journal of medical genetics. Part A  Nov 2015 
 - 2508-15 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.37248  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Child, Preschool<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 3--genetics<br/>Facies<br/>Female<br/>Genes, Recessive<br/>Genetic Association Studies<br/>Homozygote<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Intellectual Disability--complications<br/>Male<br/>Muscle Weakness--complications<br/>Pedigree<br/>Siblings<br/>Syndrome