TY  - GEN
AU  - Laffargue,Fanny
AU  - Bourthoumieu,Sylvie
AU  - Llanas,Brigitte
AU  - Baudouin,Véronique
AU  - Lahoche,Annie
AU  - Morin,Denis
AU  - Bessenay,Lucie
AU  - De Parscau,Loïc
AU  - Cloarec,Sylvie
AU  - Delrue,Marie-Ange
AU  - Taupiac,Emmanuelle
AU  - Dizier,Emilie
AU  - Laroche,Cécile
AU  - Bahans,Claire
AU  - Yardin,Catherine
AU  - Lacombe,Didier
AU  - Guigonis,Vincent
TI  - Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome
SN  - 1468-2044
PY  - 2015///0528
KW  - Adolescent
KW  - Central Nervous System Diseases
KW  - complications
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 17
KW  - genetics
KW  - Dental Enamel
KW  - abnormalities
KW  - Diabetes Mellitus, Type 2
KW  - Female
KW  - France
KW  - Hepatocyte Nuclear Factor 1-beta
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Infant
KW  - Kidney Diseases, Cystic
KW  - Male
KW  - Mental Disorders
KW  - Phenotype
KW  - Prospective Studies
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1136/archdischild-2014-306810
ER  -