Novel multilocus imprinting disturbances in a child with expressive language delay and intellectual disability-Reference-Cited by-同舟云学术

Novel multilocus imprinting disturbances in a child with expressive language delay and intellectual disability

Published:2022-04 Issue:7 Volume:188 Page:2209-2216
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Tayeh Marwan K.¹^ORCID,DeVaul Janean²,LeSueur Kristin²,Yang Chen²³,Bedoyan Jirair K.⁴,Thomas Peedikayil⁵,Hannibal Mark C.²,Innis Jeffrey W.²⁵^ORCID

Affiliation:

1. Department of Medical and Molecular Genetics, Division of Indiana, University Genetics Testing Laboratories Indiana University Indianapolis Indiana USA

2. Department of Pediatrics, Division of Pediatric Genetics, Metabolism and Genomic Medicine University of Michigan Ann Arbor Michigan USA

3. Department of Pathology University of Michigan Ann Arbor Michigan USA

4. Department of Pediatrics, Division of Genetic and Genomic Medicine University of Pittsburgh Pittsburgh Pennsylvania USA

5. Department of Human Genetics University of Michigan Ann Arbor Michigan USA

Funder

University of Michigan

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62752

Reference14 articles.

1. An atypical case of hypomethylation at multiple imprinted loci

2. Transient Neonatal Diabetes, ZFP57, and Hypomethylation of Multiple Imprinted Loci

3. Exceptionally mild Angelman syndrome phenotype associated with an incomplete imprinting defect

4. Preserved expressive language as a phenotypic determinant of Mosaic Angelman Syndrome

5. Disturbed methylation at multiple imprinted loci: an increasing observation in imprinting disorders

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