A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development-Reference-Cited by-同舟云学术

A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development

Published:2013-07-07 Issue:1 Volume:2 Page:7-29
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Darlow J. M.¹²,Dobson M. G.¹²,Darlay R.³,Molony C. M.⁴,Hunziker M.²⁵,Green A. J.¹⁶,Cordell H. J.³,Puri P.²⁵,Barton D. E.¹⁶

Affiliation:

1. National Centre for Medical Genetics Our Lady's Children's Hospital Crumlin Dublin 12 Ireland

2. National Children's Research Centre Our Lady's Children's Hospital Crumlin Dublin 12 Ireland

3. Institute of Genetic Medicine Newcastle University Newcastle upon Tyne United Kingdom

4. Merck & Co. Inc 1 Merck Drive Whitehouse Station New Jersey 08889

5. National Children's Hospital Tallaght Dublin 24 Ireland

6. University College Dublin UCD School of Medicine and Medical Sciences Our Lady's Children's Hospital Crumlin Dublin 12 Ireland

Funder

The Children's Medical and Research Foundation

Our Lady's Children's Hospital

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.22

Reference114 articles.

1. Merlin—rapid analysis of dense genetic maps using sparse gene flow trees

2. Quantification of type I error probabilities for heterogeneity LOD scores

3. A complex regulatory network of transcription factors critical for ocular development and disease

4. Expression of estrogen induced gene 121-like (EIG121L) during early Xenopus development

5. Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24

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