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One or more keywords matched the following properties of KOCHEL, ROBIN
PropertyValue
keywords autism spectrum disorder; ASD; developmental delays; diagnosis; phenotype; genotype; regression; skill loss; vaccines; parent perceptions
One or more keywords matched the following items that are connected to KOCHEL, ROBIN
Item TypeName
Academic Article Expanding the clinical spectrum of the 16p11.2 chromosomal rearrangements: three patients with syringomyelia.
Academic Article The MTHFR 677C-->T polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlations.
Academic Article A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Concept Phenotype
Academic Article Expression of the broad autism phenotype in simplex autism families from the Simons Simplex Collection.
Academic Article Level of functioning in autism spectrum disorders: phenotypic congruence among affected siblings.
Academic Article The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Academic Article Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication.
Academic Article The complex behavioral phenotype of 15q13.3 microdeletion syndrome.
Academic Article The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.
Academic Article Clinical phenotype of the recurrent 1q21.1 copy-number variant.
Academic Article Simons Variation in Individuals Project (Simons VIP): a genetics-first approach to studying autism spectrum and related neurodevelopmental disorders.
Academic Article The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications.
Academic Article Erratum to: The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications.
Academic Article Developmental trajectories for young children with 16p11.2 copy number variation.
Academic Article Gene Disrupting Mutations Associated with Regression in Autism Spectrum Disorder.
Academic Article Neurocognitive and Neurobehavioral Phenotype of Youth with Schaaf-Yang Syndrome.
Search Criteria
  • Phenotype