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E Rajcan-Separovic

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Clinical Genetics|February 29, 2012

Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disabilityY Qiao, C Tyson, M Hrynchak, et al.

American Journal of Medical Genetics. Part A|November 12, 2005

Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGHC Tyson, C Harvard, R Locker, et al.

American Journal of Medical Genetics. Part A|February 13, 2009

Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disabilityC Tyson, A J Dawson, S Bal, et al.

Clinical Epigenetics|November 6, 2019

A genome-wide DNA methylation signature for SETD1B-related syndromeI M Krzyzewska, S M Maas, P Henneman, et al.

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Search research articles

Showing results (21-30 of 24) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 24 results.

Clinical Genetics|February 29, 2012

Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disabilityY Qiao, C Tyson, M Hrynchak, et al.

American Journal of Medical Genetics. Part A|November 12, 2005

Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGHC Tyson, C Harvard, R Locker, et al.

American Journal of Medical Genetics. Part A|February 13, 2009

Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disabilityC Tyson, A J Dawson, S Bal, et al.

Clinical Epigenetics|November 6, 2019

A genome-wide DNA methylation signature for SETD1B-related syndromeI M Krzyzewska, S M Maas, P Henneman, et al.

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