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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2002 | 1 |
2004 | 1 |
2012 | 1 |
2014 | 1 |
2016 | 1 |
2017 | 1 |
2024 | 0 |
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Page 1
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease.
Am J Hum Genet. 2017 Jan 5;100(1):75-90. doi: 10.1016/j.ajhg.2016.12.003. Epub 2016 Dec 29.
Am J Hum Genet. 2017.
PMID: 28041643
Free PMC article.
Strategies for genetic study of hearing loss in the Brazilian northeastern region.
Melo US, Santos S, Cavalcanti HG, Andrade WT, Dantas VG, Rosa MR, Mingroni-Netto RC.
Melo US, et al.
Int J Mol Epidemiol Genet. 2014 Feb 17;5(1):11-21. eCollection 2014.
Int J Mol Epidemiol Genet. 2014.
PMID: 24596593
Free PMC article.
Item in Clipboard
Two novel disease-causing mutations in the CLRN1 gene in patients with Usher syndrome type 3.
García-García G, Aparisi MJ, Rodrigo R, Sequedo MD, Espinós C, Rosell J, Olea JL, Mendívil MP, Ramos-Arroyo MA, Ayuso C, Jaijo T, Aller E, Millán JM.
García-García G, et al.
Mol Vis. 2012;18:3070-8. Epub 2012 Dec 29.
Mol Vis. 2012.
PMID: 23304067
Free PMC article.
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Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability.
Aller E, Jaijo T, Oltra S, Alió J, Galán F, Nájera C, Beneyto M, Millán JM.
Aller E, et al.
Clin Genet. 2004 Dec;66(6):525-9. doi: 10.1111/j.1399-0004.2004.00352.x.
Clin Genet. 2004.
PMID: 15521980
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USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses.
Adato A, Vreugde S, Joensuu T, Avidan N, Hamalainen R, Belenkiy O, Olender T, Bonne-Tamir B, Ben-Asher E, Espinos C, Millán JM, Lehesjoki AE, Flannery JG, Avraham KB, Pietrokovski S, Sankila EM, Beckmann JS, Lancet D.
Adato A, et al.
Eur J Hum Genet. 2002 Jun;10(6):339-50. doi: 10.1038/sj.ejhg.5200831.
Eur J Hum Genet. 2002.
PMID: 12080385
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