Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome. [electronic resource]
Producer: 20150528Description: 259-64 p. digitalISSN:- 1468-2044
- 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
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.