BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 8084622)

  • 1. Hearing loss in Townes-Brocks syndrome.
    Rossmiller DR; Pasic TR
    Otolaryngol Head Neck Surg; 1994 Sep; 111(3 Pt 1):175-80. PubMed ID: 8084622
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A new family with the Townes-Brocks syndrome.
    de Vries-Van der Weerd MA; Willems PJ; Mandema HM; ten Kate LP
    Clin Genet; 1988 Sep; 34(3):195-200. PubMed ID: 3180506
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Townes-Brocks syndrome. Report of a case and review of the literature.
    Ferraz FG; Nunes L; Ferraz ME; Sousa JP; Santos M; Carvalho C; Maroteaux P
    Ann Genet; 1989; 32(2):120-3. PubMed ID: 2667456
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Hearing loss in Townes-Brocks syndrome].
    Rodríguez Asensio J; Rodríguez Rosell MV; Ramos Pérez A
    Acta Otorrinolaringol Esp; 2003; 54(7):518-22. PubMed ID: 14671925
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Townes-Brocks syndrome.
    Powell CM; Michaelis RC
    J Med Genet; 1999 Feb; 36(2):89-93. PubMed ID: 10051003
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Townes-Brocks syndrome with hypothyroidism.
    Goswami V; Dubey NK
    Indian Pediatr; 2007 Feb; 44(2):140-2. PubMed ID: 17351307
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Two cases of Townes-Brocks syndrome with previously undescribed anomalies.
    Marlin S; Toublanc JE; Petit C
    Clin Dysmorphol; 1998 Oct; 7(4):295-8. PubMed ID: 9823498
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Townes-Brocks syndrome in an infant with translocation t (5;16).
    Serville F; Lacombe D; Saura R; Billeaud C; Sergent MP
    Genet Couns; 1993; 4(2):109-12. PubMed ID: 8357560
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Townes-Brocks syndrome: detection of a SALL1 mutation hot spot and evidence for a position effect in one patient.
    Marlin S; Blanchard S; Slim R; Lacombe D; Denoyelle F; Alessandri JL; Calzolari E; Drouin-Garraud V; Ferraz FG; Fourmaintraux A; Philip N; Toublanc JE; Petit C
    Hum Mutat; 1999; 14(5):377-86. PubMed ID: 10533063
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Adult diagnosis of Townes-Brocks syndrome with renal failure: Two related cases and review of literature.
    Beaudoux O; Lebre AS; Doco Fenzy M; Spodenkiewicz M; Canivet E; Colosio C; Poirsier C
    Am J Med Genet A; 2021 Mar; 185(3):937-944. PubMed ID: 33438842
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Anus-hand-ear syndrome (Townes-Brocks syndrome)].
    Kurosawa K
    Ryoikibetsu Shokogun Shirizu; 2001; (33):211-2. PubMed ID: 11462405
    [No Abstract]   [Full Text] [Related]  

  • 12. Variable expressivity of renal involvement in a further family with Townes-Brocks syndrome.
    Eker HK; Balasar Ö
    Clin Dysmorphol; 2015 Jan; 24(1):24-5. PubMed ID: 25192472
    [No Abstract]   [Full Text] [Related]  

  • 13. Description of a patient with difficult nosological classification: Goldenhar syndrome or Townes-Brocks syndrome?
    Gabrielli O; Bonifazi V; Offidani AM; Cellini A; Coppa GV; Giorgi PL
    Minerva Pediatr; 1993 Nov; 45(11):459-62. PubMed ID: 8133838
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deletion upstream of SALL1 producing Townes-Brocks syndrome.
    Stevens CA; May KM
    Am J Med Genet A; 2016 Sep; 170(9):2476-8. PubMed ID: 27277004
    [No Abstract]   [Full Text] [Related]  

  • 15. Endocrine abnormalities in Townes-Brocks syndrome.
    Lawrence C; Hong-McAtee I; Hall B; Hartsfield J; Rutherford A; Bonilla T; Bay C
    Am J Med Genet A; 2013 Sep; 161A(9):2266-73. PubMed ID: 23894113
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Otologic and audiologic features of Nager acrofacial dysostosis.
    Herrmann BW; Karzon R; Molter DW
    Int J Pediatr Otorhinolaryngol; 2005 Aug; 69(8):1053-9. PubMed ID: 16005346
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Conductive hearing loss, middle ear ossicular anomalies, malformed thickened lop auricles, and micrognathia. A rare autosomal dominant congenital syndrome.
    Schweitzer VG; Kemink JL; Graham MD
    Am J Otol; 1984 Jul; 5(5):387-91. PubMed ID: 6476090
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotypic variability in Townes-Brocks syndrome.
    Monteiro de Pina-Neto J
    Am J Med Genet; 1984 May; 18(1):147-52. PubMed ID: 6741990
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Otolaryngological manifestations of cleidocranial dysplasia, concentrating on audiological findings.
    Visosky AM; Johnson J; Bingea B; Gurney T; Lalwani AK
    Laryngoscope; 2003 Sep; 113(9):1508-14. PubMed ID: 12972925
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss.
    Yang G; Yin Y; Tan Z; Liu J; Deng X; Yang Y
    BMC Med Genomics; 2021 Jan; 14(1):24. PubMed ID: 33478437
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.