Continuous hypomethylation of the KCNQ1OT1 :TSS‐DMR in monochorionic twins discordant for Beckwith‐Wiedemann syndrome-Reference-Cited by-同舟云学术

Continuous hypomethylation of the KCNQ1OT1 :TSS‐DMR in monochorionic twins discordant for Beckwith‐Wiedemann syndrome

Published:2017-08-16 Issue:10 Volume:173 Page:2847-2850
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Inoue Takanobu¹²,Nakamura Akie¹,Matsubara Keiko¹,Nyuzuki Hiromi³,Nagasaki Keisuke³,Oka Akira²,Fukami Maki¹,Kagami Masayo¹^ORCID

Affiliation:

1. Department of Molecular EndocrinologyNational Research Institute for Child Health and DevelopmentTokyoJapan

2. Department of PediatricsThe University of Tokyo HospitalTokyoJapan

3. Division of PediatricsDepartment of Homeostatic Regulation and DevelopmentNiigata University Graduate School of Medical and Dental SciencesNiigataJapan

Funder

Japan Society for the Promotion of Science

Japan Agency for Medical Research and Development

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.38419

Reference14 articles.

1. Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells

2. EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver–Russell and Beckwith–Wiedemann syndrome

3. Maternal Hypomethylation of KvDMR in a Monozygotic Male Twin Pair Discordant for Beckwith-Wiedemann Syndrome

4. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith–Wiedemann syndrome

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