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 *

205 related articles for article (PubMed ID: 12834121)

  • 21. Genetic heterogeneity in Usher syndrome.
    Keats BJ; Savas S
    Am J Med Genet A; 2004 Sep; 130A(1):13-6. PubMed ID: 15368488
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Hearing loss in Usher syndrome type II is nonprogressive.
    Reisser CF; Kimberling WJ; Otterstedde CR
    Ann Otol Rhinol Laryngol; 2002 Dec; 111(12 Pt 1):1108-11. PubMed ID: 12498372
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The Usher syndrome type 2A: clinical findings in obligate carriers.
    van Aarem A; Cremers CW; Pinckers AJ; Huygen PL; Hombergen GC; Kimberling BJ
    Int J Pediatr Otorhinolaryngol; 1995 Mar; 31(2-3):159-74. PubMed ID: 7782174
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Sector Retinitis Pigmentosa Associated With Novel Compound Heterozygous Mutations of CDH23.
    Branson SV; McClintic JI; Stamper TH; Haldeman-Englert CR; John VJ
    Ophthalmic Surg Lasers Imaging Retina; 2016 Feb; 47(2):183-6. PubMed ID: 26878454
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7A.
    Kumar A; Babu M; Kimberling WJ; Venkatesh CP
    Mol Vis; 2004 Nov; 10():910-6. PubMed ID: 15592175
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical and molecular genetics of Usher syndrome.
    Kimberling WJ; Möller C
    J Am Acad Audiol; 1995 Jan; 6(1):63-72. PubMed ID: 7696679
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Usher syndrome in four Norwegian counties.
    Grøndahl J; Mjøen S
    Clin Genet; 1986 Jul; 30(1):14-28. PubMed ID: 3757293
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q.
    Pieke-Dahl S; Möller CG; Kelley PM; Astuto LM; Cremers CW; Gorin MB; Kimberling WJ
    J Med Genet; 2000 Apr; 37(4):256-62. PubMed ID: 10745043
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The molecular genetics of Usher syndrome.
    Ahmed ZM; Riazuddin S; Riazuddin S; Wilcox ER
    Clin Genet; 2003 Jun; 63(6):431-44. PubMed ID: 12786748
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Usher syndrome type I is not linked to D1S81 (pTHH 33): evidence for genetic heterogeneity.
    Kaplan J; Guasconi G; Bonneau D; Melki J; Briard ML; Munnich A; Dufier JL; Frézal J
    Ann Genet; 1990; 33(2):105-8. PubMed ID: 1978628
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Usher syndrome clinical types I and II: could ocular symptoms and signs differentiate between the two types?
    Tsilou ET; Rubin BI; Caruso RC; Reed GF; Pikus A; Hejtmancik JF; Iwata F; Redman JB; Kaiser-Kupfer MI
    Acta Ophthalmol Scand; 2002 Apr; 80(2):196-201. PubMed ID: 11952489
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Novel mutations in MYO7A and USH2A in Usher syndrome.
    Maubaret C; Griffoin JM; Arnaud B; Hamel C
    Ophthalmic Genet; 2005 Mar; 26(1):25-9. PubMed ID: 15823922
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Carriers of the Usher syndrome type IB: is audiometric identification possible?
    Wagenaar M; Snik AF; Kimberling WJ; Cremers CW
    Am J Otol; 1996 Nov; 17(6):853-8. PubMed ID: 8915413
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Usher's syndrome type III: ENG findings in four affected and six unaffected siblings.
    Karjalainen S; Teräsvirta M; Kärjä J; Kääriäinen H
    J Laryngol Otol; 1985 Jan; 99(1):43-8. PubMed ID: 3871466
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prevalence of 2314delG mutation in Spanish patients with Usher syndrome type II (USH2).
    Beneyto MM; Cuevas JM; Millán JM; Espinós C; Mateu E; González-Cabo P; Baiget M; Doménech M; Bernal S; Ayuso C; García-Sandoval B; Trujillo MJ; Borrego S; Antiñolo G; Carballo M; Nájera C
    Ophthalmic Genet; 2000 Jun; 21(2):123-8. PubMed ID: 10916187
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Usher syndrome: a case report].
    Drouet A; Swalduz B; Guilloton L; Faivre A; Felten D
    Rev Neurol (Paris); 2003 Mar; 159(3):323-5. PubMed ID: 12703051
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum review.
    Li T; Feng Y; Liu Y; He C; Liu J; Chen H; Deng Y; Li M; Li W; Song J; Niu Z; Sang S; Wen J; Men M; Chen X; Li J; Liu X; Ling J
    Gene; 2019 Jul; 704():113-120. PubMed ID: 30974196
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Clinical presentation of DFNB12 and Usher syndrome type 1D.
    Bork JM; Morell RJ; Khan S; Riazuddin S; Wilcox ER; Friedman TB; Griffith AJ
    Adv Otorhinolaryngol; 2002; 61():145-52. PubMed ID: 12408077
    [No Abstract]   [Full Text] [Related]  

  • 39. [Mutational frequencies in usherin(USH2A gene) in 26 Colombian individuals with Usher syndrome type II].
    López G; Gelvez NY; Tamayo M
    Biomedica; 2011 Mar; 31(1):82-90. PubMed ID: 22159486
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification of three novel mutations in the MYO7A gene.
    Cuevas JM; Espinós C; Millán JM; Sánchez F; Trujillo MJ; Ayuso C; Beneyto M; Nájera C
    Hum Mutat; 1999 Aug; 14(2):181. PubMed ID: 10447383
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.