A child with autism, behavioral issues, and dysmorphic features found to have a tandem duplication within CTNND2 by mate‐pair sequencing

Author:

Miller Danny E.12ORCID,Squire Audrey1,Bennett James T.13

Affiliation:

1. Department of Pediatrics, Division of Genetic MedicineUniversity of Washington and Seattle Children's Hospital Seattle Washington

2. Department of Medicine, Division of Medical GeneticsUniversity of Washington Seattle Washington

3. Center for Developmental Biology and Regenerative MedicineSeattle Children's Research Institute Seattle Washington

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference13 articles.

1. Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia

2. Analysis of de novo copy number variations in a family affected with autism spectrum disorders using high‐resolution array‐based comparative genomic hybridization;He W.;Zhonghua Yi Xue Yi Chuan Xue Za Zhi Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics,2012

3. Improving mammalian genome scaffolding using large insert mate-pair next-generation sequencing

4. Analysis of protein‐coding genetic variation in 60,706 humans;Lek M.;Nature,2016

5. δ-catenin, an Adhesive Junction–associated Protein Which Promotes Cell Scattering

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