Targeted gene sequencing and whole-exome sequencing in autopsied fetuses with prenatally diagnosed kidney anomalies-Reference-Cited by-同舟云学术

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Targeted gene sequencing and whole-exome sequencing in autopsied fetuses with prenatally diagnosed kidney anomalies

Published:2018-02-23 Issue:4 Volume:93 Page:860-869
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Rasmussen M.¹^ORCID,Sunde L.¹²,Nielsen M.L.¹,Ramsing M.³,Petersen A.⁴,Hjortshøj T.D.⁵,Olsen T.E.⁶,Tabor A.⁷,Hertz J.M.⁸,Johnsen I.⁹,Sperling L.¹⁰,Petersen O.B.¹¹,Jensen U.B.¹²,Møller F.G.¹²,Petersen M.B.¹³¹⁴,Lildballe D.L.¹

Affiliation:

1. Department of Clinical Genetics; Aarhus University Hospital; Aarhus Denmark

2. Department of Biomedicine; Aarhus University; Aarhus Denmark

3. Department of Pathology; Randers Regional Hospital; Randers Denmark

4. Department of Pathology; Aalborg University Hospital; Aalborg Denmark

5. Department of Clinical Genetics; Rigshospitalet; Copenhagen Denmark

6. Department of Pathology; Rigshospitalet; Copenhagen Denmark

7. Department of Obstetrics, Center of Fetal Medicine; Rigshospitalet; Copenhagen Denmark

8. Department of Clinical Genetics; Odense University Hospital; Odense Denmark

9. Department of Pathology; Odense University Hospital; Odense Denmark

10. Department of Gynecology and Obstetrics; Odense University Hospital; Odense Denmark

11. Department of Gynecology and Obstetrics; Aarhus University Hospital; Aarhus Denmark

12. Department of Pediatrics; Herning Regional Hospital; Herning Denmark

13. Department of Clinical Genetics; Aalborg University Hospital; Aalborg Denmark

14. Department of Clinical Medicine; Aalborg University; Aalborg Denmark

Funder

Dansk Nefrologisk Selskab

Aarhus Universitet

The Regional Postgraduate Medical Education Office Research Fund

Carl and Ellen Hertz'

Haderslevs Foundation

Olga Madsen's foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.13185/fullpdf

Reference47 articles.

1. Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindred;Heimler;Am J Med Genet,1986

2. Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database;Bower;Hum Mutat,2012

3. Effect of drugs on renal development;Schreuder;Clin J Am Soc Nephrol,2011

4. Maternal diabetes mellitus and congenital anomalies of the kidney and urinary tract (CAKUT) in the child;Dart;Am J Kidney Dis,2015

5. Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans;Vivante;Pediatr Nephrol,2014

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