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Soorya, Latha
One or more keywords matched the following items that are connected to
Soorya, Latha
Item Type
Name
Concept
Chromosomes, Human, Pair 17
Concept
Chromosomes, Human, Pair 22
Academic Article
Complex autism spectrum disorder in a patient with a 17q12 microduplication.
Academic Article
Framework for assessing individuals with rare genetic disorders associated with profound intellectual and multiple disabilities (PIMD): the example of Phelan McDermid Syndrome.
Academic Article
Volumetric Analysis of the Basal Ganglia and Cerebellar Structures in Patients with Phelan-McDermid Syndrome.
Academic Article
Diffusion Tensor Imaging Abnormalities in the Uncinate Fasciculus and Inferior Longitudinal Fasciculus in Phelan-McDermid Syndrome.
Academic Article
Psychometric Study of the Social Responsiveness Scale in Phelan-McDermid Syndrome.
Academic Article
Shifted phase of EEG cross-frequency coupling in individuals with Phelan-McDermid syndrome.
Academic Article
Strong evidence for genotype-phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium.
Academic Article
Parent-reported measure of repetitive behavior in Phelan-McDermid syndrome.
Academic Article
Updated consensus guidelines on the management of Phelan-McDermid syndrome.
Search Criteria
Chromosomes Human