These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 33098377)

  • 21. Branchio-oto-renal syndrome.
    Kochhar A; Fischer SM; Kimberling WJ; Smith RJ
    Am J Med Genet A; 2007 Jul; 143A(14):1671-8. PubMed ID: 17238186
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Clinical symptoms of branchio-oto-renal syndrome in a family with a positive test for EYA1 gene].
    Markova TG
    Vestn Otorinolaringol; 2006; (6):25-8. PubMed ID: 17419499
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genome-wide copy number variation analysis of a Branchio-oto-renal syndrome cohort identifies a recombination hotspot and implicates new candidate genes.
    Brophy PD; Alasti F; Darbro BW; Clarke J; Nishimura C; Cobb B; Smith RJ; Manak JR
    Hum Genet; 2013 Dec; 132(12):1339-50. PubMed ID: 23851940
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Branchio-oto-renal syndrome.
    Smith RJ; Schwartz C
    J Commun Disord; 1998; 31(5):411-20; quiz 421. PubMed ID: 9777487
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndrome.
    Unzaki A; Morisada N; Nozu K; Ye MJ; Ito S; Matsunaga T; Ishikura K; Ina S; Nagatani K; Okamoto T; Inaba Y; Ito N; Igarashi T; Kanda S; Ito K; Omune K; Iwaki T; Ueno K; Yahata M; Ohtsuka Y; Nishi E; Takahashi N; Ishikawa T; Goto S; Okamoto N; Iijima K
    J Hum Genet; 2018 May; 63(5):647-656. PubMed ID: 29500469
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A novel splice site mutation in the EYA1 gene in a Korean family with branchio-oto (BO) syndrome.
    Kwon MJ; Boo SH; Kim HJ; Cho YS; Chung WH; Hong SH
    Acta Otolaryngol; 2009 Jun; 129(6):688-93. PubMed ID: 18763178
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Re-Examining the Cochlea in Branchio-Oto-Renal Syndrome: Genotype-Phenotype Correlation.
    Pao J; D'Arco F; Clement E; Picariello S; Moonis G; Robson CD; Juliano AF
    AJNR Am J Neuroradiol; 2022 Feb; 43(2):309-314. PubMed ID: 35058298
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel mutation in EYA1 in a Chinese family with Branchio-oto-renal syndrome.
    Wang YG; Sun SP; Qiu YL; Xing QH; Lu W
    BMC Med Genet; 2018 Aug; 19(1):139. PubMed ID: 30086703
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Identification of a novel mutation in the EYA1 gene in a Korean family with branchio-oto-renal (BOR) syndrome.
    Kim SH; Shin JH; Yeo CK; Chang SH; Park SY; Cho EH; Ki CS; Kim JW
    Int J Pediatr Otorhinolaryngol; 2005 Aug; 69(8):1123-8. PubMed ID: 16005355
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome.
    Wang SH; Wu CC; Lu YC; Lin YH; Su YN; Hwu WL; Yu IS; Hsu CJ
    Laryngoscope; 2012 May; 122(5):1130-6. PubMed ID: 22447252
    [TBL] [Abstract][Full Text] [Related]  

  • 31. EYA1 and SIX1 gene mutations in Japanese patients with branchio-oto-renal (BOR) syndrome and related conditions.
    Okada M; Fujimaru R; Morimoto N; Satomura K; Kaku Y; Tsuzuki K; Nozu K; Okuyama T; Iijima K
    Pediatr Nephrol; 2006 Apr; 21(4):475-81. PubMed ID: 16491411
    [TBL] [Abstract][Full Text] [Related]  

  • 32. SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR.
    Kochhar A; Orten DJ; Sorensen JL; Fischer SM; Cremers CW; Kimberling WJ; Smith RJ
    Hum Mutat; 2008 Apr; 29(4):565. PubMed ID: 18330911
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Prenatal diagnosis of a case with Branchi-oto-renal syndrome].
    Mi X; Yang S; Shen X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Dec; 36(12):1210-1212. PubMed ID: 31813150
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome.
    Hoskins BE; Cramer CH; Silvius D; Zou D; Raymond RM; Orten DJ; Kimberling WJ; Smith RJ; Weil D; Petit C; Otto EA; Xu PX; Hildebrandt F
    Am J Hum Genet; 2007 Apr; 80(4):800-4. PubMed ID: 17357085
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Branchio-otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8.
    Schmidt T; Bierhals T; Kortüm F; Bartels I; Liehr T; Burfeind P; Shoukier M; Frank V; Bergmann C; Kutsche K
    Cytogenet Genome Res; 2014; 142(1):1-6. PubMed ID: 24135068
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Branchio-oto-renal syndrome: identification of a novel mutation in the EYA1 gene.
    Rodríguez-Soriano J; Vallo A; Bilbao JR; Castaño L
    Pediatr Nephrol; 2001 Jul; 16(7):550-3. PubMed ID: 11465802
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The Cochlea in Branchio-Oto-Renal Syndrome: An Objective Method for the Diagnosis of Offset Cochlear Turns.
    Juliano AF; D'Arco F; Pao J; Picariello S; Clement E; Moonis G; Robson CD
    AJNR Am J Neuroradiol; 2022 Nov; 43(11):1646-1652. PubMed ID: 36175083
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Description of a large kindred with autosomal dominant inheritance of branchial arch anomalies, hearing loss, and ear pits, and exclusion of the branchio-oto-renal (BOR) syndrome gene locus (chromosome 8q13.3).
    Stratakis CA; Lin JP; Rennert OM
    Am J Med Genet; 1998 Sep; 79(3):209-14. PubMed ID: 9788564
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Young woman with branchio-oto-renal syndrome and a novel mutation in the EYA-1 gene.
    Nardi E; Palermo A; Cusimano P; Mulè G; Cerasola G
    Clin Nephrol; 2011 Oct; 76(4):330-3. PubMed ID: 21955869
    [TBL] [Abstract][Full Text] [Related]  

  • 40. BOR-syndrome-associated Eya1 mutations lead to enhanced proteasomal degradation of Eya1 protein.
    Musharraf A; Kruspe D; Tomasch J; Besenbeck B; Englert C; Landgraf K
    PLoS One; 2014; 9(1):e87407. PubMed ID: 24489909
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.