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Publications by S. Meunier
Study of Six Patients With Complete F9 Deletion Characterized by Cytogenetic Microarray: Role of the SOX3 Gene in Intellectual Disability
Journal of Thrombosis and Haemostasis
Medicine
Hematology
Abnormal Cerebellar Processing of the Neck Proprioceptive Information Drives Dysfunctions in Cervical Dystonia
Scientific Reports
Multidisciplinary
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Molecular Cytogenetic Study of the Nf2 Gene Deletion in Meningioma in Sudanese Patients
Balkan Journal of Medical Genetics
Genetics
Exons Deletion of CNKSR2 Gene Identified in X-Linked Syndromic Intellectual Disability
BMC Medical Genetics
Genetics
Application of Chromosome Microarray Analysis in Patients With Unexplained Developmental Delay/Intellectual Disability in South China
Pediatrics and Neonatology
Child Health
Pediatrics
Perinatology
A Dynamic Database of Microarray-Characterized Cell Lines With Various Cytogenetic and Genomic Backgrounds
G3: Genes, Genomes, Genetics
Medicine
Genetics
Molecular Biology
Genomic Aberrations of the CACNA2D1 Gene in Three Patients With Epilepsy and Intellectual Disability
European Journal of Human Genetics
Genetics
Clinical Implications of Cytogenetic Heterogeneity in Multiple Myeloma Patients With TP53 Deletion
Modern Pathology
Forensic Medicine
Pathology
The Evaluation of DiGeorge Syndrome Gene Deletion Using Molecular Cytogenetic Techniques
BMC Genomics
Biotechnology
Genetics
The Role of Social Participation in the Formation of Identity in Young People With Mild Intellectual Disability and in Intellectual Norm: A Comparative Study
Roczniki Psychologiczne
Psychology
Support Needs of Adults With Intellectual Disability Across Domains: The Role of Technology
Journal of Special Education Technology
Computer Science Applications
Education
