Urological Findings in Beckwith-Wiedemann Syndrome With Chromosomal Duplications of 11p15.5: Evaluation and Management-Reference-Cited by-同舟云学术

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Urological Findings in Beckwith-Wiedemann Syndrome With Chromosomal Duplications of 11p15.5: Evaluation and Management

Published:2017-02 Issue: Volume:100 Page:224-227
ISSN:0090-4295
Container-title:Urology
language:en
Short-container-title:Urology

Author:

Tong Carmen C.,Duffy Kelly A.,Chu David I.,Weiss Dana A.,Srinivasan Arun K.,Canning Douglas A.,Kalish Jennifer M.^ORCID

Publisher

Elsevier BV

Subject

Urology

Reference15 articles.

1. Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, management and follow-up of the syndrome;Mussa;Eur J Med Genet,2016

2. Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome;Slavotinek;J Med Genet,1997

3. Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome;Mussa;Pediatr Nephrol,2012

4. Clinical features and natural history of Beckwith-Wiedemann syndrome: presentation of 74 new cases;Elliott;Clin Genet,1994

5. Microarray based analysis of 3p25-p26 deletions (3p- syndrome);Shuib;Am J Med Genet A,2009

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3. Characterization of the Beckwith‐Wiedemann spectrum: Diagnosis and management;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2019-08-30

4. Beckwith–Wiedemann syndrome in diverse populations;American Journal of Medical Genetics Part A;2019-02-04

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