16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.

Steinman, Kyle J

16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort. [electronic resource] - American journal of medical genetics. Part A 11 2016 - 2943-2955 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1552-4833

10.1002/ajmg.a.37820 doi


Adolescent
Adult
Child
Child, Preschool
Chromosome Deletion
Chromosome Disorders--diagnosis
Chromosome Duplication
Chromosomes, Human, Pair 16
Cohort Studies
Electroencephalography
Epilepsy--diagnosis
Female
Genotype
Humans
Infant
Male
Middle Aged
Phenotype
Young Adult