BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 3740720)

  • 1. Branchio-oto-renal dysplasia in three families.
    Gimsing S; Dyrmose J
    Ann Otol Rhinol Laryngol; 1986; 95(4 Pt 1):421-6. PubMed ID: 3740720
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Branchio-oto-renal dysplasia. A hereditary dominant autosomal syndrome with variable expression].
    Stoll C; Roth MP; Hessemann H; Paira M
    Arch Fr Pediatr; 1983 Dec; 40(10):763-6. PubMed ID: 6673680
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Branchio-oto-renal dysplasia and branchio-oto dysplasia: two distinct autosomal dominant disorders.
    Melnick M; Hodes ME; Nance WE; Yune H; Sweeney A
    Clin Genet; 1978 May; 13(5):425-42. PubMed ID: 657583
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Branchio-oto-renal dysplasia and branchio-oto dysplasia: report of eight new cases.
    Martini A; Comacchio F; Candiani F; Vio S
    Am J Otol; 1987 Mar; 8(2):116-22. PubMed ID: 3591918
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic aspects of the BOR syndrome--branchial fistulas, ear pits, hearing loss, and renal anomalies.
    Fraser FC; Ling D; Clogg D; Nogrady B
    Am J Med Genet; 1978; 2(3):241-52. PubMed ID: 263442
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Branchio-oto-renal dysplasia associated with tetralogy of Fallot.
    Daggilas A; Antoniades K; Palasis S; Aidonis A
    Head Neck; 1992; 14(2):139-42. PubMed ID: 1601651
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) gene at 8q13.
    Kumar S; Marres HA; Cremers CW; Kimberling WJ
    Am J Med Genet; 1998 Apr; 76(5):395-401. PubMed ID: 9556298
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical aspects of the branchio-oto-renal syndrome.
    Smith PG; Dyches TJ; Loomis RA
    Otolaryngol Head Neck Surg; 1984 Aug; 92(4):468-75. PubMed ID: 6435070
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Malformation processes in the middle ear. Branchio-oto-renal syndrome (BOR)].
    Motta G; Mesolella M; Salafia M
    Acta Otorhinolaryngol Ital; 1996 Apr; 16(2 Suppl 53):42-6. PubMed ID: 8928671
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hemifacial microsomia and the branchio-oto-renal syndrome.
    Rollnick BR; Kaye CI
    J Craniofac Genet Dev Biol Suppl; 1985; 1():287-95. PubMed ID: 3877103
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Branchio-oto-renal syndrome (BOR syndrome). A dysplasia syndrome with branchial abnormalities, deafness and kidney disease].
    Holzmüller M
    HNO; 2000 Nov; 48(11):839-42. PubMed ID: 11139890
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Branchio-oto-renal syndrome: further delineation of an underdiagnosed syndrome.
    Chitayat D; Hodgkinson KA; Chen MF; Haber GD; Nakishima S; Sando I
    Am J Med Genet; 1992 Aug; 43(6):970-5. PubMed ID: 1415348
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss.
    Fraser FC; Sproule JR; Halal F
    Am J Med Genet; 1980; 7(3):341-9. PubMed ID: 7468659
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The earpits-deafness syndrome. Clinical and genetic aspects.
    Cremers CW; Fikkers-Van Noord M
    Int J Pediatr Otorhinolaryngol; 1980 Nov; 2(4):309-22. PubMed ID: 6964893
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Branchio-Oto-renal syndrome: a report on nine family groups.
    Bellini C; Piaggio G; Massocco D; Perfumo F; Bertini ; Gusmano R; Serra G
    Am J Kidney Dis; 2001 Mar; 37(3):505-9. PubMed ID: 11228174
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The branchio-oto-renal syndrome (report of two family groups).
    Raspino M; Tarantino V; Moni L; Verrina E; Ciardi MR; Gusmano R
    J Laryngol Otol; 1988 Feb; 102(2):138-41. PubMed ID: 3346591
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Branchio-oto-renal syndrome. 4 cases in three families].
    Basse F; Lacombe D; Abousleiman J; Pauly P; De Martin A
    Presse Med; 1995 May; 24(18):842-4. PubMed ID: 7638114
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of Branchio-Oto-Renal (BOR) syndrome.
    Kalatzis V; Sahly I; El-Amraoui A; Petit C
    Dev Dyn; 1998 Dec; 213(4):486-99. PubMed ID: 9853969
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.