Publications
L’une des missions de la FRH est de diffuser les résultats des recherches effectuées dans le domaine du handicap. Voici un recueil de publications en lien avec cette large thématique. N’hésitez pas à nous faire suivre vos publications.
Affichage de 13–24 sur 75 résultats
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16q24.1 microdeletion in a premature newborn: usefulness of array-based comparative genomic hybridation (array CGH) in persistent pulmonary hypertension of the newborn
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Une approche plurifactorielle des symptômes négatifs dans la microdélétion 22q11.2
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Deviant trajectories of cortical maturation in 22q11.2 deletion syndrome (22q11DS): A cross-sectional and longitudinal study
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Reduced Fronto-Temporal and Limbic Connectivity in the 22q11.2 Deletion Syndrome: Vulnerability Markers for Developing Schizophrenia?
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Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations
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Psychiatric Disorders and Intellectual Functioning Throughout Development in Velocardiofacial (22q11.2 Deletion) Syndrome
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Structural changes to the fusiform gyrus: A cerebral marker for social impairments in 22q11.2 deletion syndrome?
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Congenital heart disease is associated with reduced cortical and hippocampal volume in patients with 22q11.2 deletion syndrome
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Young children with Velo-Cardio-Facial syndrome (CATCH-22). Psychological and language phenotypes
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Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes
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Source monitoring for actions in adolescents with 22q11.2 deletion syndrome (22q11DS)
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Concurrent microdeletion and duplication of 22q11.2