Handicap Mental
Affichage de 37–45 sur 57 résultats
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Nineteen Additional Unpredicted Transcripts from Human Chromosome 21
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Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2
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Personnes en situation de handicap : mouvements entre milieu résidentiel et milieu ordinaire, besoins et lacunes du dispositif de prise en charge
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Perturbations of heart development and function in cardiomyocytes from human embryonic stem cells with trisomy 21
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Practical Guidelines for Managing Patients with 22q11.2 Deletion Syndrome
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Prevalence and risk of Down syndrome in monozygotic and dizygotic multiple pregnancies in Europe : implication for prenatal screening
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Psychiatric Disorders and Intellectual Functioning Throughout Development in Velocardiofacial (22q11.2 Deletion) Syndrome
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Recurrent Mutations in the CDKL5 Gene: Genotype-phenotype Relationships
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Reduced Fronto-Temporal and Limbic Connectivity in the 22q11.2 Deletion Syndrome: Vulnerability Markers for Developing Schizophrenia?