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 *

156 related articles for article (PubMed ID: 7825582)

  • 21. X-linked deafness with stapes gusher in females.
    Papadaki E; Prassopoulos P; Bizakis J; Karampekios S; Papadakis H; Gourtsoyiannis N
    Eur J Radiol; 1998 Nov; 29(1):71-5. PubMed ID: 9934561
    [TBL] [Abstract][Full Text] [Related]  

  • 22. X-linked hearing loss: two gene mutation examples provide generalizable implications for clinical care.
    Stanton SG; Griffin A; Stockley TL; Brown C; Young TL; Benteau T; Abdelfatah N
    Am J Audiol; 2014 Jun; 23(2):190-200. PubMed ID: 24687041
    [TBL] [Abstract][Full Text] [Related]  

  • 23. HRCT and MRI findings in X-linked non-syndromic deafness patients with a POU3F4 mutation.
    Gong WX; Gong RZ; Zhao B
    Int J Pediatr Otorhinolaryngol; 2014 Oct; 78(10):1756-62. PubMed ID: 25175280
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21.
    Bach I; Robinson D; Thomas N; Ropers HH; Cremers FP
    Hum Genet; 1992 Aug; 89(6):620-4. PubMed ID: 1511979
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families.
    Su Y; Gao X; Huang SS; Mao JN; Huang BQ; Zhao JD; Kang DY; Zhang X; Dai P
    BMC Med Genet; 2018 Sep; 19(1):157. PubMed ID: 30176854
    [TBL] [Abstract][Full Text] [Related]  

  • 26. X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletions.
    Huber I; Bitner-Glindzicz M; de Kok YJ; van der Maarel SM; Ishikawa-Brush Y; Monaco AP; Robinson D; Malcolm S; Pembrey ME; Brunner HG
    Hum Mol Genet; 1994 Jul; 3(7):1151-4. PubMed ID: 7981685
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Clinics in diagnostic imaging (111): X-linked congenital mixed deafness syndrome.
    Chee NW; Suhailee S; Goh J
    Singapore Med J; 2006 Sep; 47(9):822-4; quiz 825. PubMed ID: 16924369
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Two siblings with isolated large vestibular aqueduct syndrome.
    Karnwal A; Hadjihannas E; Uppal HS; Raut VV
    J Otolaryngol Head Neck Surg; 2008 Apr; 37(2):E55-8. PubMed ID: 19137659
    [No Abstract]   [Full Text] [Related]  

  • 29. HDR syndrome with a novel mutation in GATA3 mimicking a congenital X-linked stapes gusher: a case report.
    Yang A; Kim J; Ki CS; Hong SH; Cho SY; Jin DK
    BMC Med Genet; 2017 Oct; 18(1):121. PubMed ID: 29073906
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Novel mutation in the homeobox domain of transcription factor POU3F4 associated with profound sensorineural hearing loss.
    Schild C; Prera E; Lüblinghoff N; Arndt S; Aschendorff A; Birkenhäger R
    Otol Neurotol; 2011 Jun; 32(4):690-4. PubMed ID: 21555964
    [TBL] [Abstract][Full Text] [Related]  

  • 31. X-linked deafness-2 (DFNX2) phenotype associated with a paracentric inversion upstream of POU3F4.
    Anger GJ; Crocker S; McKenzie K; Brown KK; Morton CC; Harrison K; MacKenzie JJ
    Am J Audiol; 2014 Mar; 23(1):1-6. PubMed ID: 24096866
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Vestibular and hearing loss in genetic and metabolic disorders.
    Gasparini P; Estivill X; Fortina P
    Curr Opin Neurol; 1999 Feb; 12(1):35-9. PubMed ID: 10097882
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Study of complex structural variations of X-linked deafness-2 based on single-molecule sequencing.
    Jiang Y; Wu L; Huang S; Li P; Gao B; Yuan Y; Zhang S; Yu G; Gao Y; Wu H; Dai P
    Biosci Rep; 2021 Jun; 41(6):. PubMed ID: 33860785
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Perilymphatic gusher and stapes surgery. A predictable complication?
    Cremers CW; Hombergen GC; Wentges RT
    Clin Otolaryngol Allied Sci; 1983 Aug; 8(4):235-40. PubMed ID: 6652936
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Hypothalamic hamartomas and inner ear diverticula with X-linked stapes gusher syndrome - new associations?
    Anderson EA; Özütemiz C; Miller BS; Moss TJ; Nascene DR
    Pediatr Radiol; 2020 Jan; 50(1):142-145. PubMed ID: 31440883
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafness.
    Vore AP; Chang EH; Hoppe JE; Butler MG; Forrester S; Schneider MC; Smith LL; Burke DW; Campbell CA; Smith RJ
    Arch Otolaryngol Head Neck Surg; 2005 Dec; 131(12):1057-63. PubMed ID: 16365218
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Clinical and molecular genetic analysis of monozygotic twins displaying stapes gusher syndrome (DFN3)].
    Oh N; Kupka S; Mirghomizadeh F; Arold R; Zimmermann R; Blin N; Zenner HP; Pfister M
    HNO; 2003 Aug; 51(8):629-33. PubMed ID: 12942177
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
    Tranebjaerg L; Schwartz C; Eriksen H; Andreasson S; Ponjavic V; Dahl A; Stevenson RE; May M; Arena F; Barker D
    J Med Genet; 1995 Apr; 32(4):257-63. PubMed ID: 7643352
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Patient with diabetes and impaired hearing].
    García E; Sánchez R; Partida M; de Mingo ML; Calatayud M; Martínez G; Hawkins F
    Endocrinol Nutr; 2012 Mar; 59(3):220-2. PubMed ID: 22153565
    [No Abstract]   [Full Text] [Related]  

  • 40. Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal families.
    Bitner-Glindzicz M; de Kok Y; Summers D; Huber I; Cremers FP; Ropers HH; Reardon W; Pembrey ME; Malcolm S
    J Med Genet; 1994 Dec; 31(12):916-21. PubMed ID: 7891371
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.