Analysis of CDKN1C in Beckwith Wiedemann Syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference29 articles.
1. Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway
2. Multiple Mechanisms Regulate Imprinting of the Mouse Distal Chromosome 7 Gene Cluster
3. Chromosome 11p15.5 regional imprinting: comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors
4. Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith–Wiedemann and Simpson–Golabi–Behmel syndromes
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1. Familial Beckwith‐Wiedemann syndrome in a multigenerational family: Forty years of careful phenotyping;American Journal of Medical Genetics Part A;2022-11-02
2. Case Report: A Novel Deletion in the 11p15 Region Causing a Familial Beckwith–Wiedemann Syndrome;Frontiers in Genetics;2021-02-19
3. Wilms Tumor;The Hereditary Basis of Childhood Cancer;2021
4. Transcriptomic Analyses of Inner Ear Sensory Epithelia in Zebrafish;The Anatomical Record;2019-12-28
5. Diagnosis of an imprinted‐gene syndrome by a novel bioinformatics analysis of whole‐genome sequences from a family trio;Molecular Genetics & Genomic Medicine;2014-08-26
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