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Search Results to Jacob Vorstman

This is a "connection" page, showing the details of why an item matched the keywords from your search.

                     
                     

One or more keywords matched the following items that are connected to Vorstman, Jacob

Item TypeName
Concept Chromosomes, Human, Pair 16
Concept Chromosome Breakage
Concept Chromosomes, Human, Pair 11
Concept Chromosomes
Concept Chromosome Segregation
Concept Chromosome Mapping
Concept Chromosome Aberrations
Concept Chromosome Deletion
Concept Chromosome Inversion
Concept Chromosome Breakpoints
Concept Chromosome Disorders
Concept Chromosomes, Human, Pair 22
Academic Article Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism.
Academic Article MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q.
Academic Article The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms.
Academic Article Behavioral problems in relation to intelligence in children with 22q11.2 deletion syndrome: a matched control study.
Academic Article A palindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies.
Academic Article Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia.
Academic Article Detailed analysis of 22q11.2 with a high density MLPA probe set.
Academic Article Association of the PIK4CA schizophrenia-susceptibility gene in adults with the 22q11.2 deletion syndrome.
Academic Article Gene-network analysis identifies susceptibility genes related to glycobiology in autism.
Academic Article Practical guidelines for managing patients with 22q11.2 deletion syndrome.
Academic Article Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.
Academic Article Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.
Academic Article Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome.
Academic Article Explaining the variable penetrance of CNVs: Parental intelligence modulates expression of intellectual impairment caused by the 22q11.2 deletion.
Academic Article [Formula: see text]Executive functioning and its relation to ASD and ADHD symptomatology in 22q11.2 deletion syndrome.
Academic Article Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Academic Article Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
Academic Article Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2.
Academic Article [A bifid uvula in a patient with schizophrenia as a sign of 22q11 deletion syndrome].
Academic Article Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size.
Academic Article Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects.
Academic Article Psychopathology in 22q11 deletion syndrome.
Academic Article Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.
Academic Article Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins.
Academic Article A novel intronic variant in UBE3A identified by genome sequencing in a patient with an atypical presentation of Angelman syndrome.

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  • Chromosomes