Proportion of cells with paternal 11p15 uniparental disomy correlates with organ enlargement in Wiedemann-Beckwith syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference45 articles.
1. Trisomy 16 and trisomy 16 mosaicism: A review
2. The Importance of Genetic Mosaicism in Human Disease
3. Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith—Wiedemann syndrome
4. Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.
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1. Further understanding of paternal uniparental disomy in Beckwith-Wiedemann syndrome;Expert Review of Endocrinology & Metabolism;2022-11-02
2. Prenatal diagnosis and genetic counseling of uniparental disomy;Taiwanese Journal of Obstetrics and Gynecology;2022-03
3. Epigenetic Mosaicism in Genomic Imprinting Disorders;Russian Journal of Genetics;2019-10
4. Somatic Mosaicism for Paternal Uniparental Disomy of 11p15.5 Region in Adrenal and Liver Tissues in a Newborn with Atypical Beckwith–Wiedemann Syndrome;Journal of Pediatric Genetics;2019-06-11
5. Mosaicism for GNAS methylation defects associated with pseudohypoparathyroidism type 1B arose in early post-zygotic phases;Clinical Epigenetics;2018-02-06
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