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 *

131 related articles for article (PubMed ID: 1307249)

  • 1. 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]  

  • 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. 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. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: clinical and genetic implications.
    Kumar S; Deffenbacher K; Marres HA; Cremers CW; Kimberling WJ
    Am J Hum Genet; 2000 May; 66(5):1715-20. PubMed ID: 10762556
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene.
    Vincent C; Kalatzis V; Compain S; Levilliers J; Slim R; Graia F; Pereira ML; Nivelon A; Croquette MF; Lacombe D
    Hum Mol Genet; 1994 Oct; 3(10):1859-66. PubMed ID: 7849713
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Oto-facio-cervical (OFC) syndrome is a contiguous gene deletion syndrome involving EYA1: molecular analysis confirms allelism with BOR syndrome and further narrows the Duane syndrome critical region to 1 cM.
    Rickard S; Parker M; van't Hoff W; Barnicoat A; Russell-Eggitt I; Winter RM; Bitner-Glindzicz M
    Hum Genet; 2001 May; 108(5):398-403. PubMed ID: 11409867
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Branchio-oto-renal syndrome: identification of novel mutations, molecular characterization, mutation distribution, and prospects for genetic testing.
    Kumar S; Deffenbacher K; Cremers CW; Van Camp G; Kimberling WJ
    Genet Test; 1997-1998; 1(4):243-51. PubMed ID: 10464653
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.
    Haan EA; Hull YJ; White S; Cockington R; Charlton P; Callen DF
    Am J Med Genet; 1989 Apr; 32(4):490-4. PubMed ID: 2773990
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.