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 *

72 related articles for article (PubMed ID: 8092199)

  • 41. The search for branchiootorenal syndrome on chromosomes 1 and 8.
    Comeau K; Kimberling WJ; Cremers CW; Shugart Y
    Ann N Y Acad Sci; 1991; 630():288-9. PubMed ID: 1952608
    [No Abstract]   [Full Text] [Related]  

  • 42. Molecular genetics of X-linked hearing impairment.
    Brunner HG; Smeets B; Smeets D; Nelen M; Cremers CW; Ropers HH
    Ann N Y Acad Sci; 1991; 630():176-90. PubMed ID: 1683204
    [No Abstract]   [Full Text] [Related]  

  • 43. [Herrmann syndrome].
    Horikawa R
    Nihon Rinsho; 2006 Sep; Suppl 3():122-4. PubMed ID: 17022514
    [No Abstract]   [Full Text] [Related]  

  • 44. 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]  

  • 45. Novel EYA1 variants causing Branchio-oto-renal syndrome.
    Klingbeil KD; Greenland CM; Arslan S; Llamos Paneque A; Gurkan H; Demir Ulusal S; Maroofian R; Carrera-Gonzalez A; Montufar-Armendariz S; Paredes R; Elcioglu N; Menendez I; Behnam M; Foster J; Guo S; Escarfuller S; Cengiz FB; Duman D; Bademci G; Tekin M
    Int J Pediatr Otorhinolaryngol; 2017 Jul; 98():59-63. PubMed ID: 28583505
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Anatomical Changes and Audiological Profile in Branchio-oto-renal Syndrome: A Literature Review.
    Lindau TA; Cardoso AC; Rossi NF; Giacheti CM
    Int Arch Otorhinolaryngol; 2014 Jan; 18(1):68-76. PubMed ID: 25992067
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Identification of a novel nonsynonymous mutation of EYA1 disrupting splice site in a Korean patient with BOR syndrome.
    Kim HR; Song MH; Kim MA; Kim YR; Lee KY; Sonn JK; Lee J; Choi JY; Kim UK
    Mol Biol Rep; 2014 Jul; 41(7):4321-7. PubMed ID: 24590738
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. Cochlear implantation in branchio-oto-renal syndrome - A surgical challenge.
    Kameswaran M; Kumar RS; Murali S; Raghunandhan S; Karthikeyan K
    Indian J Otolaryngol Head Neck Surg; 2007 Sep; 59(3):280-3. PubMed ID: 23120453
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Renal anomalies in family members of infants with bilateral renal agenesis/adysplasia.
    Schwaderer AL; Bates CM; McHugh KM; McBride KL
    Pediatr Nephrol; 2007 Jan; 22(1):52-6. PubMed ID: 16977473
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. 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]  

  • 53. From a branchial fistula to a branchiootorenal syndrome: a case report and review of the literature.
    Senel E; Kocak H; Akbiyik F; Saylam G; Gulleroglu BN; Senel S
    J Pediatr Surg; 2009 Mar; 44(3):623-5. PubMed ID: 19302870
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Refined localization of dyschromatosis symmetrica hereditaria gene to a 9.4-cM region at 1q21-22 and a literature review of 136 cases reported in China.
    He PP; He CD; Cui Y; Yang S; Xu HH; Li M; Yuan WT; Gao M; Liang YH; Li CR; Xu SJ; Chen JJ; Chen HD; Huang W; Zhang XJ
    Br J Dermatol; 2004 Apr; 150(4):633-9. PubMed ID: 15099357
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysis.
    Ni L; Wagner MJ; Kimberling WJ; Pembrey ME; Grundfast KM; Kumar S; Daiger SP; Wells DE; Johnson K; Smith RJ
    Am J Med Genet; 1994 Jun; 51(2):176-84. PubMed ID: 8092199
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Localization of branchio-oto-renal (BOR) syndrome to a 3 Mb region of chromosome 8q.
    Wang Y; Treat K; Schroer RJ; O'Brien JE; Stevenson RE; Schwartz CE
    Am J Med Genet; 1994 Jun; 51(2):169-75. PubMed ID: 8092198
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Narrowing the genetic interval and yeast artificial chromosome map in the branchio-oto-renal region on chromosome 8q.
    Kumar S; Kimberling WJ; Lanyi A; Sumegi J; Pinnt J; Ing P; Tinley S; Marres HA; Cremers CW
    Genomics; 1996 Jan; 31(1):71-9. PubMed ID: 8808282
    [TBL] [Abstract][Full Text] [Related]  

  • 58.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 59.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 60.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.