Lethal renal anomalies in a fetus with 21q22.11‐q22.12 deletion
Author:
Affiliation:
1. Michigan State University College of Human Medicine Grand Rapids Michigan USA
2. Division of Medical Genetics Spectrum Health Grand Rapids Michigan USA
Funder
Wellcome Trust
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61868
Reference15 articles.
1. SON Controls Cell-Cycle Progression by Coordinated Regulation of RNA Splicing
2. Predictors of poor neonatal outcomes in prenatally diagnosed multicystic dysplastic kidney disease
3. A new syndrome
4. Braddock‐Carey syndrome: A 21q22 contiguous gene syndrome encompassing RUNX1;Braddock S. R.;American Journal of Medical Genetics Part A,2016
5. A 2.84 Mb deletion at 21q22.11 in a patient clinically diagnosed with marden-walker syndrome
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