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 *

100 related articles for article (PubMed ID: 8558563)

  • 1. Otofaciocervical syndrome: a sporadic patient supports splitting from the branchio-oto-renal syndrome.
    Dallapiccola B; Mingarelli R
    J Med Genet; 1995 Oct; 32(10):816-8. PubMed ID: 8558563
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Branchio-oto-renal (BOR) syndrome: variable expressivity in a five-generation pedigree.
    König R; Fuchs S; Dukiet C
    Eur J Pediatr; 1994 Jun; 153(6):446-50. PubMed ID: 8088301
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of a translocation-associated deletion defines the candidate region for the gene responsible for branchio-oto-renal syndrome.
    Kalatzis V; Abdelhak S; Compain S; Vincent C; Petit C
    Genomics; 1996 Jun; 34(3):422-5. PubMed ID: 8786145
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindred.
    Rollnick BR; Kaye CI
    Am J Med Genet; 1987 May; 27(1):233. PubMed ID: 3605200
    [No Abstract]   [Full Text] [Related]  

  • 7. Branchio-oto-renal syndrome.
    Millman B; Gibson WS; Foster WP
    Arch Otolaryngol Head Neck Surg; 1995 Aug; 121(8):922-5. PubMed ID: 7619422
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Branchio-oculo-facial syndrome: broadening the spectrum.
    McCool M; Weaver DD
    Am J Med Genet; 1994 Feb; 49(4):414-21. PubMed ID: 8160736
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Patient with an EYA1 mutation with features of branchio-oto-renal and oto-facio-cervical syndrome.
    Mercer C; Gilbert R; Loughlin S; Foulds N
    Clin Dysmorphol; 2006 Oct; 15(4):211-212. PubMed ID: 16957474
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. Refining the region of branchio-oto-renal syndrome and defining the flanking markers on chromosome 8q by genetic mapping.
    Kumar S; Kimberling WJ; Connolly CJ; Tinley S; Marres HA; Cremers CW
    Am J Hum Genet; 1994 Dec; 55(6):1188-94. PubMed ID: 7977379
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Branchio-oculo-facial and branchio-oto-renal syndromes are distinct entities.
    Lin AE; Doherty R; Lea D
    Clin Genet; 1992 Apr; 41(4):221-3. PubMed ID: 1576761
    [No Abstract]   [Full Text] [Related]  

  • 13. Phenotypic manifestations of branchio-oto-renal syndrome.
    Chen A; Francis M; Ni L; Cremers CW; Kimberling WJ; Sato Y; Phelps PD; Bellman SC; Wagner MJ; Pembrey M
    Am J Med Genet; 1995 Sep; 58(4):365-70. PubMed ID: 8533848
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1.
    Thienpont B; Dimitriadou E; Theodoropoulos K; Breckpot J; Fryssira H; Kitsiou-Tzeli S; Tzoufi M; Vermeesch JR; Syrrou M; Devriendt K
    Eur J Med Genet; 2009; 52(6):393-7. PubMed ID: 19772953
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindred.
    Heimler A; Lieber E
    Am J Med Genet; 1986 Sep; 25(1):15-27. PubMed ID: 3799714
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Family with branchial arch anomalies, hearing loss, ear and commissural lip pits, and rib anomalies. A new autosomal recessive condition: branchio-oto-costal syndrome?
    Clementi M; Mammi I; Tenconi R
    Am J Med Genet; 1997 Jan; 68(1):91-3. PubMed ID: 8986284
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Branchio-oculo-facial syndrome. Report of a new case with agenesis of cerebellar vermis.
    Mazzone D; Milana A; Carpinato C
    Eur J Pediatr; 1992 Apr; 151(4):312. PubMed ID: 1499589
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. [Branchio-oto-renal malformation syndrome (author's transl)].
    Desnos J; Larget-Piet L; Riberi P; Cleirens P; Beucher A
    Ann Otolaryngol Chir Cervicofac; 1979 Dec; 96(12):849-61. PubMed ID: 533091
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.