BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

317 related articles for article (PubMed ID: 12764852)

  • 1. [Audiologic analysis of a family with nonsyndromic genetic progressive sensorineural hearing loss].
    Ni D; Dan H; Mo J
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 1999 Apr; 34(2):77-80. PubMed ID: 12764852
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Dutch family with hearing loss linked to the DFNA20/26 locus: longitudinal analysis of hearing impairment.
    Kemperman MH; De Leenheer EM; Huygen PL; van Wijk E; van Duijnhoven G; Cremers FP; Kremer H; Cremers CW
    Arch Otolaryngol Head Neck Surg; 2004 Mar; 130(3):281-8. PubMed ID: 15023833
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1).
    Pennings RJ; Bom SJ; Cryns K; Flothmann K; Huygen PL; Kremer H; Van Camp G; Cremers CW
    Arch Otolaryngol Head Neck Surg; 2003 Apr; 129(4):421-6. PubMed ID: 12707188
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss.
    Govaerts PJ; De Ceulaer G; Daemers K; Verhoeven K; Van Camp G; Schatteman I; Verstreken M; Willems PJ; Somers T; Offeciers FE
    Am J Otol; 1998 Nov; 19(6):718-23. PubMed ID: 9831143
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Audiometric analysis of a Belgian family linked to the DFNA10 locus.
    Verstreken M; Declau F; Schatteman I; Van Velzen D; Verhoeven K; Van Camp G; Willems PJ; Kuhweide EW; Verhaert E; D'Haese P; Wuyts FL; Van de Heyning PH
    Am J Otol; 2000 Sep; 21(5):675-81. PubMed ID: 10993457
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A report on a large family with X-linked recessive nonsyndromic hereditary low frequency neuropathic hearing impairment].
    Wang Q; Cao J; Yu L; Guo W; Yu N; Yang W; Gu R
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 2002 Aug; 37(4):247-51. PubMed ID: 12772406
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic characterization of hereditary hearing impairment linked to DFNA25.
    Thirlwall AS; Brown DJ; McMillan PM; Barker SE; Lesperance MM
    Arch Otolaryngol Head Neck Surg; 2003 Aug; 129(8):830-5. PubMed ID: 12925340
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Progressive cochleovestibular impairment caused by a point mutation in the COCH gene at DFNA9.
    Bom SJ; Kemperman MH; De Kok YJ; Huygen PL; Verhagen WI; Cremers FP; Cremers CW
    Laryngoscope; 1999 Sep; 109(9):1525-30. PubMed ID: 10499067
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss.
    Talebizadeh Z; Kelley PM; Askew JW; Beisel KW; Smith SD
    Hum Mutat; 1999; 14(6):493-501. PubMed ID: 10571947
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypic characterization of a DFNA6 family showing progressive low-frequency sensorineural hearing impairment.
    Tóth T; Pfister M; Zenner HP; Sziklai I
    Int J Pediatr Otorhinolaryngol; 2006 Feb; 70(2):201-6. PubMed ID: 16043233
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial auditory neuropathy.
    Wang Q; Gu R; Han D; Yang W
    Laryngoscope; 2003 Sep; 113(9):1623-9. PubMed ID: 12972945
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family.
    Plantinga RF; Cremers CW; Huygen PL; Kunst HP; Bosman AJ
    J Assoc Res Otolaryngol; 2007 Mar; 8(1):1-7. PubMed ID: 17136632
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Monogenic nonsyndromic otosclerosis: audiological and linkage analysis in a large Greek pedigree.
    Iliadou V; Van Den Bogaert K; Eleftheriades N; Aperis G; Vanderstraeten K; Fransen E; Thys M; Grigoriadou M; Pampanos A; Economides J; Iliades T; Van Camp G; Petersen MB
    Int J Pediatr Otorhinolaryngol; 2006 Apr; 70(4):631-7. PubMed ID: 16168495
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Genetic and audiological characters of a Chinese family with non-syndromic hereditary hearing loss].
    Jin Z; Cheng J; Lu Y; Li J; Sun Y; Yuan H; Han D
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Feb; 25(4):158-61. PubMed ID: 21563462
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Progressive sensorineural hearing impairment in maternally inherited diabetes mellitus and deafness (MIDD).
    Hendrickx JJ; Mudde AH; 't Hart LM; Huygen PL; Cremers CW
    Otol Neurotol; 2006 Sep; 27(6):802-8. PubMed ID: 16788417
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary postlingual sensorineural hearing loss mapping to chromosome Xq21.
    Manolis EN; Eavey RD; Sangwatanaroj S; Halpin C; Rosenbaum S; Watkins H; Jarcho J; Seidman CE; Seidman JG
    Am J Otol; 1999 Sep; 20(5):621-6. PubMed ID: 10503584
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.
    Wu CC; Chiu YH; Chen PJ; Hsu CJ
    Ear Hear; 2007 Jun; 28(3):332-42. PubMed ID: 17485982
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Examinations of distortion product otoacoustic emission in hereditary progressive non-syndromic hearing loss].
    Ke X; Yu H; Liu Y; Gu Z; Lu Y; Li L
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 2000 Apr; 35(2):102-4. PubMed ID: 12768663
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family.
    Weegerink NJ; Huygen PL; Schraders M; Kremer H; Pennings RJ; Kunst HP
    Hear Res; 2011 Dec; 282(1-2):167-77. PubMed ID: 21893181
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Audiological findings and mitochondrial DNA mutation in a large family with matrilineal sensorineural hearing loss].
    Xing G; Bu X; Yan M; Lu L; Yang S
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 2000 Apr; 35(2):98-101. PubMed ID: 12768662
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.