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 *

123 related articles for article (PubMed ID: 1478663)

  • 1. Localization of the gene for branchiootorenal syndrome to chromosome 8q.
    Smith RJ; Coppage KB; Ankerstjerne JK; Capper DT; Kumar S; Kenyon J; Tinley S; Comeau K; Kimberling WJ
    Genomics; 1992 Dec; 14(4):841-4. PubMed ID: 1478663
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Autosomal dominant branchio-oto-renal syndrome--localization of a disease gene to chromosome 8q by linkage in a Dutch family.
    Kumar S; Kimberling WJ; Kenyon JB; Smith RJ; Marres HA; Cremers CW
    Hum Mol Genet; 1992 Oct; 1(7):491-5. PubMed ID: 1307249
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. [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]  

  • 6. 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]  

  • 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. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Branchiootorenal syndrome: A case report.
    Nasir SB; Ladan SJ; Bemu AN; Jibrin J
    Niger Postgrad Med J; 2018; 25(1):60-62. PubMed ID: 29676348
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Detection of a megabase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome (TRPS): implications for mapping and cloning the BOR gene.
    Gu JZ; Wagner MJ; Haan EA; Wells DE
    Genomics; 1996 Jan; 31(2):201-6. PubMed ID: 8824802
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. The deafness, pre-auricular sinus, external ear anomaly and commissural lip pits syndrome--otological, vestibular and radiological findings.
    Marres HA; Cremers CW; Huygen PL; Joosten FB
    J Laryngol Otol; 1994 Jan; 108(1):13-8. PubMed ID: 8133157
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Autosomal dominant branchiootorenal dysplasia.
    Melnick M; Bixler D; Silk K; Yune H; Nance WE
    Birth Defects Orig Artic Ser; 1975; 11(5):121-8. PubMed ID: 1218203
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.