Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome.
Laffargue, Fanny
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
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1468-2044
10.1136/archdischild-2014-306810 doi
Adolescent
Central Nervous System Diseases--complications
Child
Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 17--genetics
Dental Enamel--abnormalities
Diabetes Mellitus, Type 2--complications
Female
France
Hepatocyte Nuclear Factor 1-beta--genetics
Humans
In Situ Hybridization, Fluorescence
Infant
Kidney Diseases, Cystic--complications
Male
Mental Disorders--genetics
Phenotype
Prospective Studies
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
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1468-2044
10.1136/archdischild-2014-306810 doi
Adolescent
Central Nervous System Diseases--complications
Child
Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 17--genetics
Dental Enamel--abnormalities
Diabetes Mellitus, Type 2--complications
Female
France
Hepatocyte Nuclear Factor 1-beta--genetics
Humans
In Situ Hybridization, Fluorescence
Infant
Kidney Diseases, Cystic--complications
Male
Mental Disorders--genetics
Phenotype
Prospective Studies