Pages that link to "Q50305704"

The following pages link to Association of syndromic mental retardation and autism with 22q11.2 duplication (Q50305704):

Displaying 18 items.

• Genetics of Autism Spectrum Disorder: Current Status and Possible Clinical Applications (Q26771770) (← links)
• Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting (Q29616013) (← links)
• Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy (Q30235312) (← links)
• Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders (Q30439224) (← links)
• Evidence for involvement of GNB1L in autism (Q30504581) (← links)
• Mouse Models of 22q11.2-Associated Autism Spectrum Disorder (Q33988040) (← links)
• High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy (Q34084054) (← links)
• Heat shock alters the expression of schizophrenia and autism candidate genes in an induced pluripotent stem cell model of the human telencephalon (Q35149520) (← links)
• Association testing of copy number variants in schizophrenia and autism spectrum disorders (Q36217805) (← links)
• 22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development. (Q36477668) (← links)
• The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder (Q36499988) (← links)
• "Idiopathic" mental retardation and new chromosomal abnormalities (Q37691480) (← links)
• Autism spectrum disorders: the quest for genetic syndromes (Q38104700) (← links)
• 22q11.2 microduplication syndrome with associated esophageal atresia/tracheo-esophageal fistula and vascular ring (Q41785812) (← links)
• Case Report Molecular characterization of microduplication 22q11.2 in a girl with hypernasal speech (Q41934822) (← links)
• Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome? (Q42119379) (← links)
• MicroRNAs: fundamental regulators of gene expression in major affective disorders and suicidal behavior? (Q42270340) (← links)
• Modeling and Predicting Developmental Trajectories of Neuropsychiatric Dimensions Associated With Copy Number Variations (Q92338797) (← links)