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 *

258 related articles for article (PubMed ID: 21563462)

  • 21. A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family.
    Wang QJ; Li QZ; Rao SQ; Zhao YL; Yuan H; Yang WY; Han DY; Shen Y
    Laryngoscope; 2006 Jun; 116(6):944-50. PubMed ID: 16735904
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature.
    Berrettini S; Forli F; Passetti S; Rocchi A; Pollina L; Cecchetti D; Mancuso M; Siciliano G
    Biosci Rep; 2008 Feb; 28(1):49-59. PubMed ID: 18215147
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [KCNQ4 gene mutations affected a pedigree with autosomal dominant hereditary hearing loss].
    Wang Q; Cao J; Li N; Yang Y; Wang Q; Yu L; Han D; Yang W
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 2002 Oct; 37(5):343-7. PubMed ID: 12772453
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Audiometric characterization of a family with digenic autosomal, dominant, progressive sensorineural hearing loss.
    Borg E; Samuelsson E; Dahl N
    Acta Otolaryngol; 2000 Jan; 120(1):51-7. PubMed ID: 10779186
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.
    Xia J; Deng H; Feng Y; Zhang H; Pan Q; Dai H; Long Z; Tang B; Deng H; Chen Y; Zhang R; Zheng D; He Y; Xia K
    J Hum Genet; 2002; 47(12):635-40. PubMed ID: 12522684
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1.
    Payne M; Yang Z; Katz BJ; Warner JE; Weight CJ; Zhao Y; Pearson ED; Treft RL; Hillman T; Kennedy RJ; Meire FM; Zhang K
    Am J Ophthalmol; 2004 Nov; 138(5):749-55. PubMed ID: 15531309
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [From gene to disease; non-syndromic, autosomal dominant, low-frequency sensorineural hearing loss (DFNA6/14)].
    Pennings RJ; Cryns K; Huygen PL; van Camp G; Cremers CW
    Ned Tijdschr Geneeskd; 2003 Nov; 147(44):2170-2. PubMed ID: 14626834
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26.
    Mangino M; Flex E; Capon F; Sangiuolo F; Carraro E; Gualandi F; Mazzoli M; Martini A; Novelli G; Dallapiccola B
    Eur J Hum Genet; 2001 Sep; 9(9):667-71. PubMed ID: 11571554
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families.
    Alasti F; Sanati MH; Behrouzifard AH; Sadeghi A; de Brouwer AP; Kremer H; Smith RJ; Van Camp G
    Int J Pediatr Otorhinolaryngol; 2008 Feb; 72(2):249-55. PubMed ID: 18022253
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Family history, clinical features, and molecular characterization of a patient with autosomal recessive non-syndromic hearing loss].
    Düzcan F; Wollnik B; Tepeli E; Ardiç FN; Uyguner O; Bağci H
    Kulak Burun Bogaz Ihtis Derg; 2003 Sep; 11(3):85-8. PubMed ID: 14699249
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Linkage and association studies in a Malaysian family with autosomal recessive non-syndromic hearing loss.
    Farah WI; Aminuddin BS; Ruszymah BH
    Malays J Pathol; 2006 Jun; 28(1):23-33. PubMed ID: 17694956
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Forms of monosymptomatic hereditary sensorineural hearing loss and deafness in the Leipzig area].
    Oeken J; König E
    HNO; 1993 Jun; 41(6):301-10. PubMed ID: 8365917
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p.
    Van Camp G; Coucke PJ; Kunst H; Schatteman I; Van Velzen D; Marres H; van Ewijk M; Declau F; Van Hauwe P; Meyers J; Kenyon J; Smith SD; Smith RJ; Djelantik B; Cremers CW; Van de Heyning PH; Willems PJ
    Genomics; 1997 Apr; 41(1):70-4. PubMed ID: 9126484
    [TBL] [Abstract][Full Text] [Related]  

  • 34. First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.
    Vieira H; Gregory-Evans K; Lim N; Brookes JL; Brueton LA; Gregory-Evans CY
    Invest Ophthalmol Vis Sci; 2002 Aug; 43(8):2540-5. PubMed ID: 12147582
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Genetic study of sensorineural hearing loss].
    Bliumina MG; Moskovkina AG
    Genetika; 1982; 18(6):1012-7. PubMed ID: 7201942
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [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]  

  • 37. Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families.
    Kamarinos M; McGill J; Lynch M; Dahl H
    Hum Mutat; 2001 Apr; 17(4):351. PubMed ID: 11295836
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1-2q23.3.
    van Beelen E; Schraders M; Huygen PL; Oostrik J; Plantinga RF; van Drunen W; Collin RW; Kooper DP; Pennings RJ; Cremers CW; Kremer H; Kunst HP
    Hear Res; 2013 Jun; 300():10-7. PubMed ID: 23538131
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Mapping of gene underlying autosomal dominant non-syndromic hearing loss(DFNA)].
    Sun HJ; Tao R; Cheng J; Yang SZ; Cao JY; Yu LM; Hong MD; Feng GY; Dai P; Yuan HJ; Han DY; He L
    Yi Chuan; 2006 Dec; 28(12):1489-94. PubMed ID: 17138532
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Two families with phenotypically different hereditary low frequency hearing impairment: longitudinal data and linkage analysis.
    Bille M; Munk-Nielsen L; Tranebjaerg L; Parving A
    Scand Audiol; 2001; 30(4):246-54. PubMed ID: 11845993
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.