Hervé, B <br/><br/>
Low-level mosaicism of a de novo derivative chromosome 9 from a t(5;9)(q35.1;q34.3) has a major phenotypic impact.  [electronic resource] 

 -  European journal of medical genetics   
 - 346-50 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2015.04.005  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 5--genetics<br/>Chromosomes, Human, Pair 9--genetics<br/>Craniofacial Abnormalities--diagnosis<br/>Gene Deletion<br/>Gene Duplication<br/>Heart Defects, Congenital--diagnosis<br/>Histone Methyltransferases<br/>Histone-Lysine N-Methyltransferase--genetics<br/>Humans<br/>Intellectual Disability--diagnosis<br/>Intracellular Signaling Peptides and Proteins--genetics<br/>Male<br/>Mosaicism<br/>Nuclear Proteins--genetics<br/>Phenotype