Autosomal dominant duplication of the renal collecting system, hearing loss, and external ear anomalies: A new syndrome?-Reference-Cited by-同舟云学术

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Autosomal dominant duplication of the renal collecting system, hearing loss, and external ear anomalies: A new syndrome?

Published:1983-03 Issue:3 Volume:14 Page:473-478
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Fraser F. C.,Aymé S.,Halal F.,Sproule J.,Opitz John M.

Publisher

Wiley

Subject

Genetics(clinical)

Reference9 articles.

1. Familial incidence of bifid and double ureters

2. Familial nephrosis associated with deafness and congenital urinary tract anomalies in siblings

3. Genetic aspects of the BOR syndrome—branchial fistulas, ear pits, hearing loss, and renal anomalies

4. Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss

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1. Molecular biology, genetic, and epigenetics of ureteral disease;Genetics and Epigenetics of Genitourinary Diseases;2025

2. Ocular manifestations of congenital anomalies of the kidney and urinary tract (CAKUT);Pediatric Nephrology;2023-07-20

3. Auricular fistula: a review of its clinical manifestations, genetics, and treatments;Journal of Molecular Medicine;2023-07-17

4. Preauricular sinus: A comparative study between different surgical approaches;Indian Journal of Otology;2017

5. Supra-auricular versus Sinusectomy Approaches for Preauricular Sinuses;International Archives of Otorhinolaryngology;2016-04-26

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