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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2014 | 1 |
2021 | 1 |
2023 | 1 |
2024 | 0 |
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Molecular Genetic Etiology and Revisiting the Middle Ear Surgery Outcomes of Branchio-Oto-Renal Syndrome: Experience in a Tertiary Referral Center.
Otol Neurotol. 2023 Jun 1;44(5):e319-e327. doi: 10.1097/MAO.0000000000003880. Epub 2023 Apr 22.
Otol Neurotol. 2023.
PMID: 37167448
Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta-analysis.
Chen A, Song J, Acke FRE, Mei L, Cai X, Feng Y, He C.
Chen A, et al.
Clin Genet. 2021 Jul;100(1):3-13. doi: 10.1111/cge.13949. Epub 2021 Mar 21.
Clin Genet. 2021.
PMID: 33624842
Branchiootorenal spectrum disorder (BORSD) is a group of rare autosomal dominant entities characterized by branchiogenic malformations, hearing loss (HL) and renal anomalies. It comprises branchiootorenal syndrome and branchiootic syndrome, distinguished by the pres …
Branchiootorenal spectrum disorder (BORSD) is a group of rare autosomal dominant entities characterized by branchiogenic malformations, hear …
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SIX1 gene: absence of mutations in children with isolated congenital anomalies of kidney and urinary tract.
Negrisolo S, Centi S, Benetti E, Ghirardo G, Della Vella M, Murer L, Artifoni L.
Negrisolo S, et al.
J Nephrol. 2014 Dec;27(6):667-71. doi: 10.1007/s40620-014-0112-x. Epub 2014 Jun 5.
J Nephrol. 2014.
PMID: 24899122
BACKGROUND: Mutations in human SIX1 gene cause branchiootorenal or branchiootic syndrome. Six1 deficient mice exhibit uni- or bilateral renal hypoplasia or kidney agenesis. ...
BACKGROUND: Mutations in human SIX1 gene cause branchiootorenal or branchiootic syndrome. Six1 deficient mice exhibit uni- or …
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