Laffargue, Fanny <br/><br/>
Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome.  [electronic resource] 

 -  Archives of disease in childhood  Mar 2015 
 - 259-64 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-2044 
<br/><br/><label>Standard No.: </label>10.1136/archdischild-2014-306810  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Central Nervous System Diseases--complications<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 17--genetics<br/>Dental Enamel--abnormalities<br/>Diabetes Mellitus, Type 2--complications<br/>Female<br/>France<br/>Hepatocyte Nuclear Factor 1-beta--genetics<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant<br/>Kidney Diseases, Cystic--complications<br/>Male<br/>Mental Disorders--genetics<br/>Phenotype<br/>Prospective Studies