Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Biochemistry (medical),Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry
Link
http://link.springer.com/content/pdf/10.1186/s13039-019-0443-3.pdf
Reference38 articles.
1. Rasmussen M, Olsen MS, Sunde L, Sperling LS. Danish fetal medicine research G, Petersen OB. Kidney anomalies diagnosed by prenatal ultrasound screening and associated non-urinary malformations: a nationwide prevalence study. Prenat Diagn. 2016;36:847–53.
2. Nef S, Neuhaus TJ, Sparta G, Weitz M, Buder K, Wisser J, et al. Outcome after prenatal diagnosis of congenital anomalies of the kidney and urinary tract. Eur J Pediatr. 2016;175:667–76.
3. Verbitsky M, Kogon AJ, Matheson M, Hooper SR, Wong CS, Warady BA, et al. Genomic disorders and neurocognitive impairment in pediatric CKD. J Am Soc Nephrol. 2017;28:2303–9.
4. Verbitsky M, Sanna-Cherchi S, Fasel DA, Levy B, Kiryluk K, Wuttke M, et al. Genomic imbalances in pediatric patients with chronic kidney disease. J Clin Invest. 2015;125:2171–8.
5. de Bruyn R, Marks SD. Postnatal investigation of fetal renal disease. Semin Fetal Neonatal Med. 2008;13:133–41.
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